Please log in
You must be logged in to send the contact request.
Manage stand orders
Select Option
Prima Lab SA
Via Antonio Monti 7,
6828
Balerna
Switzerland
Switzerland
Submit your contact details
Provide your contact details to the exhibitor. Optionally, you may also add a personal message.
Your name, phone number, and e-mail address are subject to the submission of personal data. Messe Düsseldorf GmbH expressly points out that for a data transmission into third countries, for which no adequacy decision of the EU-commission is on hand certifying an adequate level of protection of personal data, it is not ensured that there are appropriate safeguards for the protection of personal data on hand.
An error has occurred
Please check your internet connection or try again later.
Message has been sent
Your message to the exhibitor was sent successfully.
Contact
Our range of products
Product categories
- 03 Diagnostic tests
- 03.02 Immunochemistry testing, immunology testing
- 03.02.02 Diagnostic rapid tests
Diagnostic rapid tests
- COVID-19 ANTIGEN RAPID TEST
- COVID-19 IgG/IgM RAPID TEST
- VITAMIN D TEST
- IRON FER TEST
- PROSTATE PSA TEST
- ALLERGY IgE TEST
- THYROID TSH TEST
- TETANUS TEST
- C-REACTIVE PROTEIN TEST
- FOOD INTOLERANCE TEST
- CELIAC TEST
- HELICOBACTER PYLORI TEST
- BOWEL FOB TEST
- HELICOBACTER PYLORI ANTIGEN TEST
- KIDNEYS ALBUMIN TEST
- URINARY TRACT INFECTIONS TEST
- DRUG TEST
- MENOPAUSE FSH TEST
- OVULATION LH TEST
- PREGNANCY hCG TEST
- EARLY PREGNANCY hCG TEST
- SPERM TEST
- AMNIOCHECK®
- STREP A TEST
- VAGINAL pH TEST
- GIARDIA PET TEST
- URINARY CHECK-UP PET TEST
Our products
Product category: Diagnostic rapid tests
COVID-19 ANTIGEN RAPID TEST
COVID-19 ANTIGEN RAPID TEST is a rapid assay for the qualitative detection of SARS-CoV-2 antigens present in the human nasopharynx. It is intended to be used by healthcare professionals as a first approach in the diagnosis of COVID-19 - CE certified for professional in vitro diagnostic use only.
COVID-19 ANTIGEN RAPID TEST is a rapid membrane-based lateral flow immunoassay for the qualitative detection of SARS-CoV-2 antigens in human nasopharyngeal swab specimens. Pathogen-specific antigens can be used as diagnostic markers to detect the current infection status of an individual. SARS-CoV-2, as all Coronaviruses, has several known antigens, including its Nucleocapsid phosphoprotein and Spike glycoprotein, the latter being the visible protrusions on its surface and the main protein able to attack the host cells in human body.
WHY THE NEED FOR A COVID-19 ANTIGEN TEST?
With the increase of COVID-19 cases in most parts of the world, there is a growing need for diagnostic tests that are accurate and reliable, easy to use and with quick turnaround time, in order to allow frequent testing. Tests, having such characteristics and similar to the PCR technique, have been developed, in order to facilitate the diagnosis and traceability of newly infected people: the antigen tests. Since the transmission of SARS-CoV-2 virus seems to occur days after exposure to it, when the viral load reaches its peak, the frequency of testing is increasingly important in order to slow down the spread of the pandemic. An effective surveillance approach cannot be performed using the standard PCR technique because, after collection, PCR samples usually require transport to specialised laboratories run by experts, this in turn requires one or more days for the results, creates a bottleneck and is expensive. This is why the need for highly sensitive and specific devices such as the antigen tests, which open the door to effective population-wide monitoring.
HOW TO USE IT
1) Insert the sterile swab through the nostril parallel to the palate, until the contact with the nasopharynx. Gently rub and roll the swab and take it out from the nasal cavity.
2) Insert the swab into the provided extraction buffer and rotate it for about 10 seconds. Remove the swab while squeezing the sides of the tube in order to extract as much liquid as possible.
3) Add 3 drops of the extracted specimen to the sample well. Wait 15 minutes and read the results.
COVID-19 ANTIGEN RAPID TEST is a rapid membrane-based lateral flow immunoassay for the qualitative detection of SARS-CoV-2 antigens in human nasopharyngeal swab specimens. Pathogen-specific antigens can be used as diagnostic markers to detect the current infection status of an individual. SARS-CoV-2, as all Coronaviruses, has several known antigens, including its Nucleocapsid phosphoprotein and Spike glycoprotein, the latter being the visible protrusions on its surface and the main protein able to attack the host cells in human body.
WHY THE NEED FOR A COVID-19 ANTIGEN TEST?
With the increase of COVID-19 cases in most parts of the world, there is a growing need for diagnostic tests that are accurate and reliable, easy to use and with quick turnaround time, in order to allow frequent testing. Tests, having such characteristics and similar to the PCR technique, have been developed, in order to facilitate the diagnosis and traceability of newly infected people: the antigen tests. Since the transmission of SARS-CoV-2 virus seems to occur days after exposure to it, when the viral load reaches its peak, the frequency of testing is increasingly important in order to slow down the spread of the pandemic. An effective surveillance approach cannot be performed using the standard PCR technique because, after collection, PCR samples usually require transport to specialised laboratories run by experts, this in turn requires one or more days for the results, creates a bottleneck and is expensive. This is why the need for highly sensitive and specific devices such as the antigen tests, which open the door to effective population-wide monitoring.
HOW TO USE IT
1) Insert the sterile swab through the nostril parallel to the palate, until the contact with the nasopharynx. Gently rub and roll the swab and take it out from the nasal cavity.
2) Insert the swab into the provided extraction buffer and rotate it for about 10 seconds. Remove the swab while squeezing the sides of the tube in order to extract as much liquid as possible.
3) Add 3 drops of the extracted specimen to the sample well. Wait 15 minutes and read the results.
Product category: Diagnostic rapid tests
COVID-19 IgG/IgM RAPID TEST
COVID-19 IgG/IgM RAPID TEST is a rapid assay for the qualitative detection of IgG and IgM antibodies against SARS-CoV-2 in human whole blood, serum or plasma specimens. It is intended to be used by healthcare professionals as a first approach in the diagnosis of COVID-19 - CE cerified for professional in vitro diagnostic use only.
COVID-19 IgG/IgM RAPID TEST is a qualitative membrane based lateral flow immunochromatographic assay for the detection of Immunoglobulin G (IgG) and Immunoglobulin M (IgM) against SARS-CoV-2 in whole blood, serum or plasma specimens. Immunoglobulins, or antibodies, are proteins produced by specific immune cells in response to bacteria, viruses, microorganisms and other substances recognized by the body as foreign antigens. There are five classes of immunoglobulins, of which IgM are generally produced as the body’s first response to a new infection, providing short-term protection. The concentration of these antibodies increases for a few weeks and then decreases at the end of the infection. IgG, on the other hand, account for about 70 80% of immunoglobulins in the blood and they are generally produced later than the IgM. IgG levels usually tend to increase for a few weeks and then stabilise. The body is able to remember the different IgG levels, which can then be reproduced at each exposure to the same antigen.
WHY THE NEED FOR A COVID-19 SEROLOGICAL TEST?
The use of a serological test allows to identify individuals possibly exposed to the virus and to take initial precautionary isolation measures in order to reduce further spread of the virus itself. In infected individuals the incubation period can vary between 1 and 14 days, with a prevalence of 3 to 7 days, after which the first symptoms begin to appear. Sethuraman et al. show the trend over time in the detection of diagnostic tests for SARS-CoV-2. In case of nasopharyngeal swab, the detection increases after the onset of the first symptoms, reaching a peak of detection in the first week after the onset of symptoms and then decreases steadily. IgM and IgG antibodies to SARS-CoV-2 appear in the blood of infected individuals from a few days up to 2 weeks after these symptoms and, while IgM levels decrease after the end of the infection, IgG levels remain high and detectable. For this reason, these tests are useful for:
a) help the diagnosis of late symptomatic cases, as a support for molecular testing (nasopharyngeal swabs followed by PCR tests)
b) screen asymptomatic individuals who may have recently been exposed to the virus
c) assist in seroprevalence investigations to define population exposure levels.
HOW TO USE IT
1) Take a sample of whole blood after pricking the finger with the sterile lancet, taking care not to squeeze the pipette bulb. Alternatively, a laboratory micropipette can be used.
2) Deposit the blood sample into the sample well of the cassette.
3) Add 2 drops of diluent. Wait 10 minutes and read the results.
COVID-19 IgG/IgM RAPID TEST is a qualitative membrane based lateral flow immunochromatographic assay for the detection of Immunoglobulin G (IgG) and Immunoglobulin M (IgM) against SARS-CoV-2 in whole blood, serum or plasma specimens. Immunoglobulins, or antibodies, are proteins produced by specific immune cells in response to bacteria, viruses, microorganisms and other substances recognized by the body as foreign antigens. There are five classes of immunoglobulins, of which IgM are generally produced as the body’s first response to a new infection, providing short-term protection. The concentration of these antibodies increases for a few weeks and then decreases at the end of the infection. IgG, on the other hand, account for about 70 80% of immunoglobulins in the blood and they are generally produced later than the IgM. IgG levels usually tend to increase for a few weeks and then stabilise. The body is able to remember the different IgG levels, which can then be reproduced at each exposure to the same antigen.
WHY THE NEED FOR A COVID-19 SEROLOGICAL TEST?
The use of a serological test allows to identify individuals possibly exposed to the virus and to take initial precautionary isolation measures in order to reduce further spread of the virus itself. In infected individuals the incubation period can vary between 1 and 14 days, with a prevalence of 3 to 7 days, after which the first symptoms begin to appear. Sethuraman et al. show the trend over time in the detection of diagnostic tests for SARS-CoV-2. In case of nasopharyngeal swab, the detection increases after the onset of the first symptoms, reaching a peak of detection in the first week after the onset of symptoms and then decreases steadily. IgM and IgG antibodies to SARS-CoV-2 appear in the blood of infected individuals from a few days up to 2 weeks after these symptoms and, while IgM levels decrease after the end of the infection, IgG levels remain high and detectable. For this reason, these tests are useful for:
a) help the diagnosis of late symptomatic cases, as a support for molecular testing (nasopharyngeal swabs followed by PCR tests)
b) screen asymptomatic individuals who may have recently been exposed to the virus
c) assist in seroprevalence investigations to define population exposure levels.
HOW TO USE IT
1) Take a sample of whole blood after pricking the finger with the sterile lancet, taking care not to squeeze the pipette bulb. Alternatively, a laboratory micropipette can be used.
2) Deposit the blood sample into the sample well of the cassette.
3) Add 2 drops of diluent. Wait 10 minutes and read the results.
Product category: Diagnostic rapid tests
VITAMIN D TEST
VITAMIN D TEST is a CE certified rapid self-test for the semi-quantitative detection of Vitamin D in human whole blood.
VITAMIN D TEST is an immunochromatographic assay that, thanks to specific antibodies, is able to detect the levels of 25-hydroxyvitamin D in blood sample and highlight its concentration thanks to the intensity of the Test Line (T) obtained. Results in 10 minutes.
Overall Accuracy: 93,8%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a drop of blood by massaging the finger and collect it with the plastic pipette, until the dotted line.
3) Put the drop of blood on the specimen well on the test cassette.
4) Add the diluent in the buffer well, wait for 10 minutes and read the result.
VITAMIN D TEST is an immunochromatographic assay that, thanks to specific antibodies, is able to detect the levels of 25-hydroxyvitamin D in blood sample and highlight its concentration thanks to the intensity of the Test Line (T) obtained. Results in 10 minutes.
Overall Accuracy: 93,8%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a drop of blood by massaging the finger and collect it with the plastic pipette, until the dotted line.
3) Put the drop of blood on the specimen well on the test cassette.
4) Add the diluent in the buffer well, wait for 10 minutes and read the result.
Product category: Diagnostic rapid tests
IRON FER TEST
IRON FER TEST is a CE certified self-test for the detection of ferritin levels in whole blood samples.
IRON FER TEST is an immunochromatographic assay which detects the protein Ferritin thanks to special monoclonal gold-conjugate antibodies embedded to test strip. Cut-off 30 ng/mL and results in 5 minutes.
Overall Accuracy: 96,6%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 5 minutes and read the result.
IRON FER TEST is an immunochromatographic assay which detects the protein Ferritin thanks to special monoclonal gold-conjugate antibodies embedded to test strip. Cut-off 30 ng/mL and results in 5 minutes.
Overall Accuracy: 96,6%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 5 minutes and read the result.
Product category: Diagnostic rapid tests
PROSTATE PSA TEST
PROSTATE PSA TEST is a CE certified self-test for the determination of the Prostate-Specific Antigen (PSA) in whole blood samples.
PROSTATE PSA TEST is an immunochromatographic assay which detects the PSA thanks to special monoclonal gold-conjugate antibodies embedded to test strip. Results in 5 minutes.
Overall Accuracy: 90,7%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 5 minutes and read the result.
PROSTATE PSA TEST is an immunochromatographic assay which detects the PSA thanks to special monoclonal gold-conjugate antibodies embedded to test strip. Results in 5 minutes.
Overall Accuracy: 90,7%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 5 minutes and read the result.
Product category: Diagnostic rapid tests
ALLERGY IgE TEST
ALLERGY IgE is a CE certified self-test for the determination of total class E Immunoglobulins (IgE) in whole blood samples.
ALLERGY IgE TEST is an immunochromatographic test that detects the presence of IgE antibodies in the blood in concentrations above average, using special monoclonal antibodies conjugated with gold and integrated into the reactive strip. Results in 5 minutes.
Overall Accuracy: 92,4%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 5 minutes and read the result.
ALLERGY IgE TEST is an immunochromatographic test that detects the presence of IgE antibodies in the blood in concentrations above average, using special monoclonal antibodies conjugated with gold and integrated into the reactive strip. Results in 5 minutes.
Overall Accuracy: 92,4%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 5 minutes and read the result.
Product category: Diagnostic rapid tests
THYROID TSH TEST
THYROID TSH TEST is a CE certified self-test for the determination of the levels of thyroid-stimulating hormone (TSH) in whole blood samples.
THYROID TSH TEST is an immunochromatographic assay which detects the protein TSH thanks to special monoclonal gold-conjugate antibodies embedded to test strip. Cut-off 5 μIU/mL. Results in 10 minutes.
Overall Accuracy: 95%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 10 minutes and read the result.
THYROID TSH TEST is an immunochromatographic assay which detects the protein TSH thanks to special monoclonal gold-conjugate antibodies embedded to test strip. Cut-off 5 μIU/mL. Results in 10 minutes.
Overall Accuracy: 95%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 10 minutes and read the result.
Product category: Diagnostic rapid tests
TETANUS TEST
TETANUS TEST is a CE certified self-test for the determination of the level of antibodies (class G Immunoglobulins – IgG) against tetanus in whole blood samples.
TETANUS TEST is an immunochromatographic assay which detects the presence of specific antibodies IgG against tetanic toxin thanks to special monoclonal goldconjugate antibodies embedded inside the test strip. Results in 5 minutes.
Overall Accuracy: 94%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 5 minutes and read the result.
TETANUS TEST is an immunochromatographic assay which detects the presence of specific antibodies IgG against tetanic toxin thanks to special monoclonal goldconjugate antibodies embedded inside the test strip. Results in 5 minutes.
Overall Accuracy: 94%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 5 minutes and read the result.
Product category: Diagnostic rapid tests
C-REACTIVE PROTEIN TEST
C-REACTIVE PROTEIN TEST is a CE certified self-test for the detection of C-Reactive Protein (CRP) levels in blood.
C-REACTIVE PROTEIN TEST is an immunochromatographic assay which detects the CRP level thanks to special monoclonal gold-conjugate antibodies embedded to test strip. Results in 5 minutes.
Overall Accuracy: 98%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the blood collected with the pipette into the opened dropper vial.
4) Add the diluent, wait for 5 minutes and read the result.
C-REACTIVE PROTEIN TEST is an immunochromatographic assay which detects the CRP level thanks to special monoclonal gold-conjugate antibodies embedded to test strip. Results in 5 minutes.
Overall Accuracy: 98%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the blood collected with the pipette into the opened dropper vial.
4) Add the diluent, wait for 5 minutes and read the result.
Product category: Diagnostic rapid tests
FOOD INTOLERANCE TEST
FOOD INTOLERANCE TEST is a sample collection kit for detection of 64/90/120 food intolerances in blood.
FOOD INTOLERANCE TEST is performed on the sample by a specialized laboratory through an ELISA method in order to specifically detect if antibodies (IgG) against 64/90/120 different food are present into the blood sample.
HOW TO USE IT
1) Clean the end of the forefinger or of the middle finger. Massage the end of the finger, from the base of the finger to the end, to enhance the blood flow. Press the lancet, on the side from where the cap was extracted, against the fingertip. The tip retracts automatically after use.
2) Help the spillage of blood by applying pressure on the fingertip, as shown in the picture below.
3) Deposit a generous blood drop within the circle on the absorbent pad but without pressing the fingertip against the membrane. The blood sample must cover the whole absorbing membrane.
4) Fill the form included with the kit and sign it. Put the the absorbent pad card into the plastic bag supplied, close the zip and ship together with the form into the pre-printed envelope included. Mail it within the same day. After the laboratory has analyzed your sample, the report with the results will be sent to you, along with nutritional advices.
FOOD INTOLERANCE TEST is performed on the sample by a specialized laboratory through an ELISA method in order to specifically detect if antibodies (IgG) against 64/90/120 different food are present into the blood sample.
HOW TO USE IT
1) Clean the end of the forefinger or of the middle finger. Massage the end of the finger, from the base of the finger to the end, to enhance the blood flow. Press the lancet, on the side from where the cap was extracted, against the fingertip. The tip retracts automatically after use.
2) Help the spillage of blood by applying pressure on the fingertip, as shown in the picture below.
3) Deposit a generous blood drop within the circle on the absorbent pad but without pressing the fingertip against the membrane. The blood sample must cover the whole absorbing membrane.
4) Fill the form included with the kit and sign it. Put the the absorbent pad card into the plastic bag supplied, close the zip and ship together with the form into the pre-printed envelope included. Mail it within the same day. After the laboratory has analyzed your sample, the report with the results will be sent to you, along with nutritional advices.
Product category: Diagnostic rapid tests
CELIAC TEST
CELIAC TEST is a CE certified elf-test for the detection of Deamidated Gliadin Peptide (DGP) antibodies (anti-DGP), IgA and IgG in blood.
CELIAC TEST is based on an immunochromatographic reaction. If the antibodies (IgA and IgG) are present into the sample, they will react with the deamidated gliadin. A positive result means that the concentration of antibodies is nearby to 20 U/mL. Results in 10 minutes.
Overall Accuracy: 90%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 10 minutes and read the result.
CELIAC TEST is based on an immunochromatographic reaction. If the antibodies (IgA and IgG) are present into the sample, they will react with the deamidated gliadin. A positive result means that the concentration of antibodies is nearby to 20 U/mL. Results in 10 minutes.
Overall Accuracy: 90%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 10 minutes and read the result.
Product category: Diagnostic rapid tests
HELICOBACTER PYLORI TEST
HELICOBACTER PYLORI TEST is a CE certified Self-test for the determination of anti Helicobacter pylori antibodies in whole blood samples.
HELICOBACTER PYLORI TEST is an immunochromatographic test that detects the presence of anti-Helicobater pylori IgG antibodies in the blood, using special monoclonal antibodies conjugated with gold and integrated into the reactive strip. Results in 5 minutes.
Overall Accuracy: 87%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 5 minutes and read the result
HELICOBACTER PYLORI TEST is an immunochromatographic test that detects the presence of anti-Helicobater pylori IgG antibodies in the blood, using special monoclonal antibodies conjugated with gold and integrated into the reactive strip. Results in 5 minutes.
Overall Accuracy: 87%
HOW TO USE IT
1) The sample is a blood drop taken with the sterile lancet contained in the box.
2) Obtain a big drop of blood by massaging the finger and collect it with the plastic pipette.
3) Put the drop of blood on the indicated point on the device.
4) Add the diluent, wait for 5 minutes and read the result
Product category: Diagnostic rapid tests
BOWEL FOB TEST
BOWEL FOB TEST is a CE certified self-test for the detection of faecal occult blood - FOB.
BOWEL FOB TEST is an immunochromatographic test that detects the smallest amounts of blood in stool samples by using highly specific monoclonal antibodies. These properties mean that the BOWEL FOB TEST does not require particular dietary restrictions before being carried out. Results in 5 minutes.
Overall Accuracy: 92,6%
HOW TO USE IT
1) Attach the two adhesive surfaces of the stool-collecting sheet on the toilet seat surface.
2) Dip the stick into the faeces in three different points of the sample.
3) Screw on the cap, immersing the stick in the stool extraction liquid, and shake the vial.
4) Break the end of the red cap, freeing the dropper portion. Dispense 3 drops of the diluted stool sample in the well shown on the strip.
BOWEL FOB TEST is an immunochromatographic test that detects the smallest amounts of blood in stool samples by using highly specific monoclonal antibodies. These properties mean that the BOWEL FOB TEST does not require particular dietary restrictions before being carried out. Results in 5 minutes.
Overall Accuracy: 92,6%
HOW TO USE IT
1) Attach the two adhesive surfaces of the stool-collecting sheet on the toilet seat surface.
2) Dip the stick into the faeces in three different points of the sample.
3) Screw on the cap, immersing the stick in the stool extraction liquid, and shake the vial.
4) Break the end of the red cap, freeing the dropper portion. Dispense 3 drops of the diluted stool sample in the well shown on the strip.
Product category: Diagnostic rapid tests
HELICOBACTER PYLORI ANTIGEN TEST
HELICOBACTER PYLORI ANTIGEN TEST is a CE certified self-test for the detection of the Helicobacter pylori antigen in stools sample.
HELICOBACTER PYLORI ANTIGEN TEST is an immunochromatographic test that detects the presence of specific Helicobacter pylori antigens in stools by using special monoclonal antibodies conjugated with gold and integrated into the reactive strip. Results in 5 minutes.
Overall Accuracy: 92,6%
HOW TO USE IT
1) Attach the two adhesive surfaces of the stool-collecting sheet on the toilet seat surface.
2) Dip the stick into the faeces in three different points of the sample.
3) Screw on the cap, immersing the stick in the stool extraction liquid, and shake the vial.
4) Break the end of the red cap, freeing the dropper portion. Dispense 3 drops of the diluted stool sample in the well shown on the strip.
HELICOBACTER PYLORI ANTIGEN TEST is an immunochromatographic test that detects the presence of specific Helicobacter pylori antigens in stools by using special monoclonal antibodies conjugated with gold and integrated into the reactive strip. Results in 5 minutes.
Overall Accuracy: 92,6%
HOW TO USE IT
1) Attach the two adhesive surfaces of the stool-collecting sheet on the toilet seat surface.
2) Dip the stick into the faeces in three different points of the sample.
3) Screw on the cap, immersing the stick in the stool extraction liquid, and shake the vial.
4) Break the end of the red cap, freeing the dropper portion. Dispense 3 drops of the diluted stool sample in the well shown on the strip.
Product category: Diagnostic rapid tests
KIDNEYS ALBUMIN TEST
KIDNEYS ALBUMIN TEST is a CE certified self-test for the detection of Albumin in urine.
KIDNEYS ALBUMIN TEST is an immunochromatographic assay which detects the albumin protein in urine thanks to special monoclonal gold-conjugate antibodies embedded to test strip. Results in 5 minutes.
Overall Accuracy: 96,9%
HOW TO USE IT
1) The sample is the first urine of the day collected in a clean cup contained in the box.
2) Take the strip-test from the grip side.
3) Dip the strip-test for few seconds.
4) Wait for 5 minutes and read the result.
KIDNEYS ALBUMIN TEST is an immunochromatographic assay which detects the albumin protein in urine thanks to special monoclonal gold-conjugate antibodies embedded to test strip. Results in 5 minutes.
Overall Accuracy: 96,9%
HOW TO USE IT
1) The sample is the first urine of the day collected in a clean cup contained in the box.
2) Take the strip-test from the grip side.
3) Dip the strip-test for few seconds.
4) Wait for 5 minutes and read the result.
Product category: Diagnostic rapid tests
URINARY TRACT INFECTIONS TEST
URINARY TRACT INFECTIONS TEST is a CE certified self-test for the detection of leukocytes,
blood, nitrites and proteins in urine.
URINARY TRACT INFECTIONS TEST detects the presence of non-phisiological levels of leukocytes, blood, nitrites and proteins in urine thanks to specifc chemical reactions which are visibile with a colour change of the reactive area. Results in 2 minutes.
Overall Accuracy:
a) Leukocytes 97,6%
b) Blood 96%
c) Protein 88%
d) Nitrite 100%
HOW TO USE IT
1) The collection should be done with the first urine of the day.
2) Each area of the test strip checks 4 different parameters.
3) Dip the strip-test for 1-2 seconds.
4) Wait for 2 minutes then check the colours of the strip test.
blood, nitrites and proteins in urine.
URINARY TRACT INFECTIONS TEST detects the presence of non-phisiological levels of leukocytes, blood, nitrites and proteins in urine thanks to specifc chemical reactions which are visibile with a colour change of the reactive area. Results in 2 minutes.
Overall Accuracy:
a) Leukocytes 97,6%
b) Blood 96%
c) Protein 88%
d) Nitrite 100%
HOW TO USE IT
1) The collection should be done with the first urine of the day.
2) Each area of the test strip checks 4 different parameters.
3) Dip the strip-test for 1-2 seconds.
4) Wait for 2 minutes then check the colours of the strip test.
Product category: Diagnostic rapid tests
DRUG TEST
DRUG TEST is a self-test for the detection of 6 drugs in urine: Morphine, Amphetamine, Cocaine, Marijuana, Methamphetamine and Methadone.
DRUG TEST Panel is an immunochromatographic assay that can be performed without the use of an instrument. The test utilizes monoclonal antibodies to selectively detect levels of specific drugs in urine. Results in 5 minutes.
Overall Accuracy:
a) Amphetamine (AMP) 98%
b) Methamhetamine (MET) 97,2%
c) Cocaine (COC) 98%
d) Morphine (MOP) 95,2%
e) Methadone (MTD) 98,8%
f) Marijuana (THC) 98%
HOW TO USE IT
1) With the arrow pointing toward the urine specimen, dip the test panel vertically in the urine specimen for at least 10 to 15 seconds.
2) Replace the cap and place the test panel on a non-absorbent flat surface.
3) Start the timer and wait for the coloured line(s) to appear.
DRUG TEST Panel is an immunochromatographic assay that can be performed without the use of an instrument. The test utilizes monoclonal antibodies to selectively detect levels of specific drugs in urine. Results in 5 minutes.
Overall Accuracy:
a) Amphetamine (AMP) 98%
b) Methamhetamine (MET) 97,2%
c) Cocaine (COC) 98%
d) Morphine (MOP) 95,2%
e) Methadone (MTD) 98,8%
f) Marijuana (THC) 98%
HOW TO USE IT
1) With the arrow pointing toward the urine specimen, dip the test panel vertically in the urine specimen for at least 10 to 15 seconds.
2) Replace the cap and place the test panel on a non-absorbent flat surface.
3) Start the timer and wait for the coloured line(s) to appear.
Product category: Diagnostic rapid tests
MENOPAUSE FSH TEST
MENOPAUSE FSH TEST is a CE cerified self-test for the determination of the Follicle Stimulating Hormone - FSH in urine.
MENOPAUSE FSH TEST is an immunochromatographic test that detects FSH through special goldconjugated monoclonal antibodies included in the reactive strip. Cut-off 25 mIU/mL. Results in 5 minutes.
Overall Accuracy: 94%
HOW TO USE IT
1) Remove the protective cap - this exposes the absorbing tip.
2) Place the absorbing tip right under the flow of urine for at least 10 seconds.
3) Alternatively if easier, urine can be collected in a clean, dry, residue-free container and the absorbing tip can be dipped into the urine for 10 seconds.
4) Place the protective cap back onto the absorbing tip. Wait for 5 minutes and read the result.
MENOPAUSE FSH TEST is an immunochromatographic test that detects FSH through special goldconjugated monoclonal antibodies included in the reactive strip. Cut-off 25 mIU/mL. Results in 5 minutes.
Overall Accuracy: 94%
HOW TO USE IT
1) Remove the protective cap - this exposes the absorbing tip.
2) Place the absorbing tip right under the flow of urine for at least 10 seconds.
3) Alternatively if easier, urine can be collected in a clean, dry, residue-free container and the absorbing tip can be dipped into the urine for 10 seconds.
4) Place the protective cap back onto the absorbing tip. Wait for 5 minutes and read the result.
Product category: Diagnostic rapid tests
OVULATION LH TEST
OVULATION LH TEST is a CE certified self-test for the detection of the LH level in urine.
OVULATION LH TEST is an immunochromatographic test that detects LH through special goldconjugated monoclonal antibodies included in the reactive strip. Cut-off 25 mIU/mL. Results in 5 minutes.
Overall Accuracy 94,4%
HOW TO USE IT
1) Remove the protective cap - this exposes the absorbing tip.
2) Place the absorbing tip right under the flow of urine for at least 10 seconds.
3) Alternatively if easier, urine can be collected in a clean, dry, residue-free container and the absorbing tip can be dipped into the urine for 10 seconds.
4) Place the protective cap back onto the absorbing tip. Wait for 5 minutes and read the result.
OVULATION LH TEST is an immunochromatographic test that detects LH through special goldconjugated monoclonal antibodies included in the reactive strip. Cut-off 25 mIU/mL. Results in 5 minutes.
Overall Accuracy 94,4%
HOW TO USE IT
1) Remove the protective cap - this exposes the absorbing tip.
2) Place the absorbing tip right under the flow of urine for at least 10 seconds.
3) Alternatively if easier, urine can be collected in a clean, dry, residue-free container and the absorbing tip can be dipped into the urine for 10 seconds.
4) Place the protective cap back onto the absorbing tip. Wait for 5 minutes and read the result.
Product category: Diagnostic rapid tests
PREGNANCY hCG TEST
PREGNANCY hCG TEST is a CE certified self-test for detecting the Chorionic Gonadotropin hormone (hCG) in urine.
PREGNANCY HCG TEST is an immunochromatographic device that detects hCG hormone through special goldconjugated monoclonal antibodies included in the reactive strip. Cut-off 25 mIU/mL. Results in 5 minutes.
Overall Accuracy 98,9%
HOW TO USE IT
1) Remove the protective cap - this exposes the absorbing tip.
2) Place the absorbing tip right under the flow of urine for at least 10 seconds.
3) Alternatively if easier, urine can be collected in a clean, dry, residue-free container and the absorbing tip can be dipped into the urine for 10 seconds.
4) Place the protective cap back onto the absorbing tip. Wait for 5 minutes and read the result.
PREGNANCY HCG TEST is an immunochromatographic device that detects hCG hormone through special goldconjugated monoclonal antibodies included in the reactive strip. Cut-off 25 mIU/mL. Results in 5 minutes.
Overall Accuracy 98,9%
HOW TO USE IT
1) Remove the protective cap - this exposes the absorbing tip.
2) Place the absorbing tip right under the flow of urine for at least 10 seconds.
3) Alternatively if easier, urine can be collected in a clean, dry, residue-free container and the absorbing tip can be dipped into the urine for 10 seconds.
4) Place the protective cap back onto the absorbing tip. Wait for 5 minutes and read the result.
Product category: Diagnostic rapid tests
EARLY PREGNANCY hCG TEST
EARLY PREGNANCY hCG TEST is a CE certified self-test for the early detection of the hCG in human urine sample.
EARLY PREGNANCY TEST is an immunochromatographic assay for the early detection of hCG hormone in urine by using a combination of one monoclonal-dye conjugate and another one monoclonal-solid phase antibody to selectively identify hCG in test samples. Cut-off 10 mIU/mL. Results in 5 minutes.
Overall Accuracy 100%
HOW TO USE IT
1) Remove the protective cap - this exposes the absorbing tip.
2) Place the absorbing tip right under the flow of urine for at least 10 seconds.
3) Alternatively if easier, urine can be collected in a clean, dry, residue-free container and the absorbing tip can be dipped into the urine for 10 seconds.
4) Place the protective cap back onto the absorbing tip. Wait for 5 minutes and read the result.
EARLY PREGNANCY TEST is an immunochromatographic assay for the early detection of hCG hormone in urine by using a combination of one monoclonal-dye conjugate and another one monoclonal-solid phase antibody to selectively identify hCG in test samples. Cut-off 10 mIU/mL. Results in 5 minutes.
Overall Accuracy 100%
HOW TO USE IT
1) Remove the protective cap - this exposes the absorbing tip.
2) Place the absorbing tip right under the flow of urine for at least 10 seconds.
3) Alternatively if easier, urine can be collected in a clean, dry, residue-free container and the absorbing tip can be dipped into the urine for 10 seconds.
4) Place the protective cap back onto the absorbing tip. Wait for 5 minutes and read the result.
Product category: Diagnostic rapid tests
SPERM TEST
SPERM TEST is a CE certified self-test for in vitro qualitative estimation of sperm concentration in human semen.
SPERM TEST is biochemical assay for in vitro qualitative estimation of sperm concentration in human semen. Sperm cells are trapped on the first surface layer of the membrane, while a staining solution is used to dye sperm cells. The darker is the colour of well A, the higher is the sperm concentration. If the colour of well A is lighter than the standard colour of reference well B, it means that the concentration of sperm is less than 15 million/mL. If the colour of well A test is darker than the standard colour of reference well B, it means that the sperm concentration is greater than 15 million/mL. Results in 2 minutes.
Overall Accuracy 99,1%
HOW TO USE IT
1) Collect the semen directly into the collection cup. Shake the semen evenly in the collection cup and leave it to stand for 15 minutes at room temperature until the semen liquefies.
2) Using the pipette provided in the foil pouch, dispense one drop of semen into test well A.
3) Once the semen is soaked into well A, add three drops of the blue staining solution to well A. Let it soak for 1-2 minutes.
4) Add two drops of the transparent washing solution to well A, and let it soak for 1-2 minutes, and then read the results immediately. Read the colour of well B, comparing the colour of A to B.
SPERM TEST is biochemical assay for in vitro qualitative estimation of sperm concentration in human semen. Sperm cells are trapped on the first surface layer of the membrane, while a staining solution is used to dye sperm cells. The darker is the colour of well A, the higher is the sperm concentration. If the colour of well A is lighter than the standard colour of reference well B, it means that the concentration of sperm is less than 15 million/mL. If the colour of well A test is darker than the standard colour of reference well B, it means that the sperm concentration is greater than 15 million/mL. Results in 2 minutes.
Overall Accuracy 99,1%
HOW TO USE IT
1) Collect the semen directly into the collection cup. Shake the semen evenly in the collection cup and leave it to stand for 15 minutes at room temperature until the semen liquefies.
2) Using the pipette provided in the foil pouch, dispense one drop of semen into test well A.
3) Once the semen is soaked into well A, add three drops of the blue staining solution to well A. Let it soak for 1-2 minutes.
4) Add two drops of the transparent washing solution to well A, and let it soak for 1-2 minutes, and then read the results immediately. Read the colour of well B, comparing the colour of A to B.
Product category: Diagnostic rapid tests
AMNIOCHECK®
AMNIOCHECK® is a CE certified rapid test for the detection of amniotic fluid leak and identification of wetness cause during pregnancy.
AMNIOCHECK® changes colours when it comes in contact with fluid of pH levels greater than or equal to 6.5 units. Amniotic fluid pH levels are greater than 6.5. The panty liner is specific to vaginal fluid, and if contaminated with urine, in the range of pH 5.5-7.0, will not give a positive result (combination of the chemical formulation and panty liner composition reduces interference from urine and therefore increase specificity). Results in 15 minutes.
HOW TO USE IT
1) Attach the panty liner to the underwear. Wear it as a normal panty liner till feel wetness (do not exceed 12 hours).
2) At the first sense of wetness, remove the panty liner and wait up to 15 minutes and check for a colour change on the panty liner. The detection panty liner is specific to vaginal fluid, and if contaminated with urine it will not give a positive result.
AMNIOCHECK® changes colours when it comes in contact with fluid of pH levels greater than or equal to 6.5 units. Amniotic fluid pH levels are greater than 6.5. The panty liner is specific to vaginal fluid, and if contaminated with urine, in the range of pH 5.5-7.0, will not give a positive result (combination of the chemical formulation and panty liner composition reduces interference from urine and therefore increase specificity). Results in 15 minutes.
HOW TO USE IT
1) Attach the panty liner to the underwear. Wear it as a normal panty liner till feel wetness (do not exceed 12 hours).
2) At the first sense of wetness, remove the panty liner and wait up to 15 minutes and check for a colour change on the panty liner. The detection panty liner is specific to vaginal fluid, and if contaminated with urine it will not give a positive result.
Product category: Diagnostic rapid tests
STREP A TEST
STREP A TEST is a CE certified Self-test for the detection of Group A ß-hemolytic streptococcus bacteria in throat infection.
STREP A TEST is an immunochromatographic test that detects the presence of specific Streptococcus A antigens in troat swab samples by using special monoclonal antibodies. Results in 5 minutes.
Overall Accuracy 97,1%
HOW TO USE IT
1) Collect a throat sample using the supplied swab and the tongue depressor.
2) Insert the absorbent cotton tip of the swab into the extraction tube placed on the workstation and add the two diluent Solutions.
3) Mix the solution and leave the swab inside the tube for 2-5 minutes of incubation. Then remove the swab and squeeze the cotton tip to collect as much liquid as possible.
4) Apply the provided dropper to the tube and dispense 1 drop into the well in the test case. Note: If the dispensed drop contains air bubbles, add another drop to the well.
STREP A TEST is an immunochromatographic test that detects the presence of specific Streptococcus A antigens in troat swab samples by using special monoclonal antibodies. Results in 5 minutes.
Overall Accuracy 97,1%
HOW TO USE IT
1) Collect a throat sample using the supplied swab and the tongue depressor.
2) Insert the absorbent cotton tip of the swab into the extraction tube placed on the workstation and add the two diluent Solutions.
3) Mix the solution and leave the swab inside the tube for 2-5 minutes of incubation. Then remove the swab and squeeze the cotton tip to collect as much liquid as possible.
4) Apply the provided dropper to the tube and dispense 1 drop into the well in the test case. Note: If the dispensed drop contains air bubbles, add another drop to the well.
Product category: Diagnostic rapid tests
VAGINAL pH TEST
VAGINAL pH TEST is a CE certified self-test for the semiquantitative determination of pH in female vaginal swab specimens.
A pH paper is used to determine pH levels in specimen obtained through a vaginal swab. As soon as the swab containing the specimen from vagina comes in contact with the pH paper encased in the test panel, a colour change occurs. Different pH levels can result in different grades and shades of colour with each colour grade/shade specifying a particular pH level on the colour scale. Cut-off 3.8-7.0. Results in less than 1 minute.
Overall Accuracy 98,6%
HOW TO USE IT
1) Insert the head of swab gently into the vagina and gently press the swab to a point for approximately 10 seconds. It is important to ensure that the head of swab becomes well moistened with vaginal secretions. Withdraw the swab from the vagina for testing. Apply the head of swab onto pH area of the test panel for at least 5 times, make sure enough secretion is applied on the pH area of the test panel.
2) Read the result immediately while the measurement zone is still wet. Compare the colour in the pH measurement zone with the colour scale on the foil pouch.
A pH paper is used to determine pH levels in specimen obtained through a vaginal swab. As soon as the swab containing the specimen from vagina comes in contact with the pH paper encased in the test panel, a colour change occurs. Different pH levels can result in different grades and shades of colour with each colour grade/shade specifying a particular pH level on the colour scale. Cut-off 3.8-7.0. Results in less than 1 minute.
Overall Accuracy 98,6%
HOW TO USE IT
1) Insert the head of swab gently into the vagina and gently press the swab to a point for approximately 10 seconds. It is important to ensure that the head of swab becomes well moistened with vaginal secretions. Withdraw the swab from the vagina for testing. Apply the head of swab onto pH area of the test panel for at least 5 times, make sure enough secretion is applied on the pH area of the test panel.
2) Read the result immediately while the measurement zone is still wet. Compare the colour in the pH measurement zone with the colour scale on the foil pouch.
Product category: Diagnostic rapid tests
GIARDIA PET TEST
GIARDIA PET TEST is a rapid test for the qualitative identification of Giardia lamblia antigens in animal faeces.
GIARDIA PET TEST is a lateral flow immunochromatographic rapid assay for the qualitative identification of Giardia lamblia antigens in animal faeces. During testing, a specimen is applied into the sample well on the cassette test. Giardia antigens, if present in the specimen, react with anti-Giardia antibodies coated colloidal gold particles in the test strip. Results in 10 minutes.
HOW TO USE IT
1) Collect the sample and dip the stick into faeces in different points.
2) Screw on the cap, put the stick in the stool extraction liquid and shake the vial.
3) Apply 2 drops of the diluent stool sample.
4) Wait 10 minutes and read the result.
GIARDIA PET TEST is a lateral flow immunochromatographic rapid assay for the qualitative identification of Giardia lamblia antigens in animal faeces. During testing, a specimen is applied into the sample well on the cassette test. Giardia antigens, if present in the specimen, react with anti-Giardia antibodies coated colloidal gold particles in the test strip. Results in 10 minutes.
HOW TO USE IT
1) Collect the sample and dip the stick into faeces in different points.
2) Screw on the cap, put the stick in the stool extraction liquid and shake the vial.
3) Apply 2 drops of the diluent stool sample.
4) Wait 10 minutes and read the result.
Product category: Diagnostic rapid tests
URINARY CHECK-UP PET TEST
URINARY CHECK-UP PET TEST is a pet urinary screening test.
URINARY CHECK-UP PET TEST contains plastic strips on which are applied 10 test areas. The test is intended for qualitative and semi-quantitative analysis of 10 parameters in animal urine, such as: bilirubin, blood, glucose, ketones, pH, proteins, specific gravity, urobilinogen, leukocytes and nitrites. Urinalysis is an important tool in pet disease detection, as well as monitoring and screening animal health. Abnormalities can be indicative of diseases of urinary system as well as other organ systems, including liver function, acid-base balance and carbohydrate metabolism. Results in 2 minutes.
HOW TO USE IT
1) Collect the urine sample in a clean and dry container.
2) Each strip area tests 10 different parameters.
3) Immerse the strip-test for 1-2 seconds.
4) Wait for 2 minutes then check the colours of the strip-test.
URINARY CHECK-UP PET TEST contains plastic strips on which are applied 10 test areas. The test is intended for qualitative and semi-quantitative analysis of 10 parameters in animal urine, such as: bilirubin, blood, glucose, ketones, pH, proteins, specific gravity, urobilinogen, leukocytes and nitrites. Urinalysis is an important tool in pet disease detection, as well as monitoring and screening animal health. Abnormalities can be indicative of diseases of urinary system as well as other organ systems, including liver function, acid-base balance and carbohydrate metabolism. Results in 2 minutes.
HOW TO USE IT
1) Collect the urine sample in a clean and dry container.
2) Each strip area tests 10 different parameters.
3) Immerse the strip-test for 1-2 seconds.
4) Wait for 2 minutes then check the colours of the strip-test.
About us
Company details
PRIMA Lab SA is a Biotech Swiss Company developing simple and precise CE certified diagnostic in vitro medical devices, for a rapid check of people’s health and their pets.
PRIMA also offers rapid tests for health care professionals, providing point of care analysis to improve their services. Prevention has never been so simple, handy and accessible to everybody and everywhere: in just 5-10 minutes you can get an accurate answer about your health status and that of your pet.
Stay healthy, live better with PRIMA.
PRIMA also offers rapid tests for health care professionals, providing point of care analysis to improve their services. Prevention has never been so simple, handy and accessible to everybody and everywhere: in just 5-10 minutes you can get an accurate answer about your health status and that of your pet.
Stay healthy, live better with PRIMA.
Company data
Export content> 75%
Number of employees20-49
Area of businessDiagnostics