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Zhuhai Encode Medical Engineering Co., Ltd
No. 20, Honghui 2nd Road, Hongqi Industr Zone, Jiwan District,
519090
Zhuhai
China
China
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Contact
Gillian Xu
International sales
NO.020, Honghui 2nd Road, Hongqi Industrial Zone, Jinwan District, Zhuhai,P.R. China 519090
Zhuhai
Phone
+86 13798973089(whatsapp,wechat) +86 18575612272
Email
itd05@encode.com.cn
Emily Wu
Sales Manager
NO.020, Honghui 2nd Road, Hongqi Industrial Zone, Jinwan District, Zhuhai,P.R. China 519090
Phone
+86 13825625670
Email
itd@encode.com.cn
Bella Zeng
International sales
NO.020,Honghui 2nd RD Hongqi Industrial Zone, Jinwan District,Zhuhai,P.R China
Phone
+86 18675617122
Email
itd02@encode.com.cn
Jeniffer Zheng
International sales
NO.020,Honghui 2nd RD Hongqi Industrial Zone, Jinwan District,Zhuhai,P.R China
Phone
+86 18675617155
Email
itd03@encode.com.cn
Visit us
16.11.2020
Topic
15:30 - 16:30
Test Operation of Covid-19 IgG/IgM Rapid Test and Covid-19 Antigen Rapid Test
Zhuhai Encode Medical Engineering Co., Ltd Produce more than 9,000,000tests Covid-19 IgG/IgM Rapid Test since
February,the quality is highly recognized from customers and Covid-19 Antigen Rapid Test with 94% clinical sensitivity ,with CE and ISO approved,more details please see the product categories.
In order to help customers to visually and quickly see our package and know more about the test procedure,we operate the Covid-19 IgG/IgM test and Covid-19 Antigen test procedure in our laboratory during 15:30-16:30(Chinese time) on 16th November.
Welcome customer to visit our spot testing and give us comments!
Thanks and best regards
February,the quality is highly recognized from customers and Covid-19 Antigen Rapid Test with 94% clinical sensitivity ,with CE and ISO approved,more details please see the product categories.
In order to help customers to visually and quickly see our package and know more about the test procedure,we operate the Covid-19 IgG/IgM test and Covid-19 Antigen test procedure in our laboratory during 15:30-16:30(Chinese time) on 16th November.
Welcome customer to visit our spot testing and give us comments!
Thanks and best regards
Our range of products
Product categories
- 03 Diagnostic tests
- 03.02 Immunochemistry testing, immunology testing
- 03.02.02 Diagnostic rapid tests
Diagnostic rapid tests
- SARS-COV-2 Antigen Rapid Test
- SARS-CoV-2 IgG/IgM Rapid Test
- Flu A+B/SARS-COV-2 Antigens Multiplex Rapid Test Kit
- Influenza A+B Antigen Combo Rapid Test Kit
- Virus Sampling Tube and Swab VTM UTM
- Dengue IgG IgM/NS1 Combo Rapid Test Kit
- Sexually Chlamydia Rapid Test Kit
- Sexually HIV1/2 Rapid Test Kit
- Drugs of Abuse DOA Rapid Test Kit
- Typhoid IgG/IgM Rapid Test Kit
- Bi-state Blood Culture Bottle for the qualitative detection of microorganisms
- ToRCH Toxo/Rubella/CMV/HSV1/2 IgG/IgM Rapid Test Kit
- HCV Rapid Test Kit
- iGFBP-1 PROM Rapid Test Kit
- Strep A Rapid Test Kit
- Malaria Pf/Pan Antigen Rapid Test Kit
- Helicobacter Pylori HP Ag Self Rapid Test Kit
- 10 parameter Urinalysis reagent test strip
- Mycoplasma Identification Susceptibility Test Kit (Freeze-dried)
- Quantitative POCT fluorescence immunoassay analyzer
- Encode Produce more than 115 items of in vitro diagnostic tests
Our products
Product category: Diagnostic rapid tests
SARS-COV-2 Antigen Rapid Test
SARS-COV-2 Antigen Rapid Test Advantages:
Package:Cassette,20T/box
Storage and Validity:Store at 2-30℃ for 24 months
Test Procedure:
1. Remove the test from its sealed pouch, and place it on a clean, level surface. Label the device with patient or control identification. For best results, the assay should be performed within one hour.
2. Gently mix Extraction reagent solution.
Add 10-11 drops (about 300ul) of the Extraction Solution into the Extraction tube.
3. Place the patient swab specimen into the Extraction Tube. Roll the swab at least 10 times while pressing the swab against the bottom and side of the Extraction Tube. Leave the swab in the extraction tube for one mintues, Roll the swab head against the inside of the Extraction Tube as you remove it. Try to release as much liquid as possible. Dispose of the used swab in accordance with your biohazard waste disposal protocol.
4. Put on the tube tip, then add 2 drops (about 70-80ul) of extracted sample into the sample well. Do not handle or move the Test Device until the test is complete and ready for reading.
5. As the test begins to work, color will migrate across the membrane. Wait for the colored band(s) to appear. The result should be read at 15 minutes. Do not interpret the result after 20 minutes.
- 95% Sensitivity and 100% Specificity
- CE,ISO13485 Certificated,Ministry of Commerce Export White List
- All necessary reagent provided,no equipment needed
- Shorter the window period,Covid-19 infected can be detected within 1-3 days.
Package:Cassette,20T/box
Storage and Validity:Store at 2-30℃ for 24 months
Test Procedure:
1. Remove the test from its sealed pouch, and place it on a clean, level surface. Label the device with patient or control identification. For best results, the assay should be performed within one hour.
2. Gently mix Extraction reagent solution.
Add 10-11 drops (about 300ul) of the Extraction Solution into the Extraction tube.
3. Place the patient swab specimen into the Extraction Tube. Roll the swab at least 10 times while pressing the swab against the bottom and side of the Extraction Tube. Leave the swab in the extraction tube for one mintues, Roll the swab head against the inside of the Extraction Tube as you remove it. Try to release as much liquid as possible. Dispose of the used swab in accordance with your biohazard waste disposal protocol.
4. Put on the tube tip, then add 2 drops (about 70-80ul) of extracted sample into the sample well. Do not handle or move the Test Device until the test is complete and ready for reading.
5. As the test begins to work, color will migrate across the membrane. Wait for the colored band(s) to appear. The result should be read at 15 minutes. Do not interpret the result after 20 minutes.
Product category: Diagnostic rapid tests
SARS-CoV-2 IgG/IgM Rapid Test
SARS-CoV-2 IgG/IgM Rapid Test Advantage:
Package:Cassette,25Tests/Box
Storage and Validity:Store at 2-30℃ for 24 months
Test Procedure:
1. Bring the specimen and test components to room temperature if refrigerated or frozen. Place the test device on a clean, flat surface and label specimen number.
2. Fill the pipette dropper with the specimen. Holding the dropper vertically, dispense 1 drop (about 10 µL) of whole blood,serum, plasma into the sample well,making sure that there are no air bubbles. Then add 1-2 drops (about 70-100 µL) of Sample Diluent immediately.
Set up timer. Results can be read in 15 minutes. Don’t read result after 15 minutes.
- The First Batch of companies to List in Chinese Export White List
- Recommended by <The Lancet>, clinical result showed Sensitivity is 98%, Specificity is 100%. link:https://www.thelancet.com/journals/lanres/article/PIIS2213-2600(20)30315-5/fulltext#seccestitle160
- Certified by CE, ISO13485, Approval by South Korea ,Singapore,Philippines,France ,Ecuador, Estonia , United Kingdom etc
- *Exported more than 21 countries with 9 milliions tests, verified by the worldwide laboratories
Package:Cassette,25Tests/Box
Storage and Validity:Store at 2-30℃ for 24 months
Test Procedure:
1. Bring the specimen and test components to room temperature if refrigerated or frozen. Place the test device on a clean, flat surface and label specimen number.
2. Fill the pipette dropper with the specimen. Holding the dropper vertically, dispense 1 drop (about 10 µL) of whole blood,serum, plasma into the sample well,making sure that there are no air bubbles. Then add 1-2 drops (about 70-100 µL) of Sample Diluent immediately.
Set up timer. Results can be read in 15 minutes. Don’t read result after 15 minutes.
Product category: Diagnostic rapid tests
Flu A+B/SARS-COV-2 Antigens Multiplex Rapid Test Kit
- High sensitivity and Specificity
- Specimen:nasal swab/throat swab/nasal aspirate
- 15 minutes read the result
vitro qualitative detection of antigens to FluA/FluB/SARS-COV-2 in human nasopharyngeal secretion or oropharyngeal
secretion.
Package:20Tests/Box
Storage:Store at 2-30℃ for 24 months
Test Procedure:
1.Add all of one single buffer(400ul) into single use extraction tube.
2. Insert the specimen collection swab into the extraction tube which contains 400ul of the buffer and rotate the swab
constantly. Repeat several times and process for 2 minutes.
3. squeeze the swab on the tube wall so that the liquid is extruded continuously. Take out the sample and discard the
swab according to the treatment of infected items.
4. Cover the extraction tube with its dispensing tip. (The test result of the kit will not be affected if the treated sample
is used within 60 minutes)
Remove the test kit from the sealed foil pouch and place it on a clean and level surface.
5. Two drops of treated samples were added vertically to each of the three sample well of the test kit.
6. Wait 15 minutes to interpret and record the test result. The result is invalid after 15 minutes.
Product category: Diagnostic rapid tests
Influenza A+B Antigen Combo Rapid Test Kit
High sensitivity and Specificity
Specimen:nasal swab/throat swab/nasal aspirate
15 minutes read the result
Intended Use:
The Influenza A+B Rapid Test Device is a rapid chromatographic immunoassay for the qualitative detection of influenza A and B antigens in nasal swab or throat swab or nasal aspirate specimens. It is intended to aid in the rapid differential diagnosis of influenza A and B viral infections.
Package:20Tests/Box
Storage:Store at 2-30℃ for 24 months
Test Procedure:
1. Remove the test Device from the sealed foil pouch and use it as soon as possible. Best results will be obtained if the assay is performed immediately after opening the foil pouch.
2. Hold the extraction tube upside down vertically. Add 8-10 drops of solution to the extraction tube.
3. Place the swab specimen in the Extraction Tube. Squeeze the tube and twirl the swab 10 seconds, make sure the specimen release into the extraction buffer as much as possible. discard the swab and cover the extraction tube with dropper.
4. Add 2-3 full drops of solution to the specimen well (S) and then start the timer.
5. Read the result at 15 minutes. Do not interpret the result after 15 minutes.
Note: Very low concentrations of Flu A antigen might result in a weak line appearing in the test line regions after an extended period of time; therefore, do not read results after 15 minutes.
Specimen:nasal swab/throat swab/nasal aspirate
15 minutes read the result
Intended Use:
The Influenza A+B Rapid Test Device is a rapid chromatographic immunoassay for the qualitative detection of influenza A and B antigens in nasal swab or throat swab or nasal aspirate specimens. It is intended to aid in the rapid differential diagnosis of influenza A and B viral infections.
Package:20Tests/Box
Storage:Store at 2-30℃ for 24 months
Test Procedure:
1. Remove the test Device from the sealed foil pouch and use it as soon as possible. Best results will be obtained if the assay is performed immediately after opening the foil pouch.
2. Hold the extraction tube upside down vertically. Add 8-10 drops of solution to the extraction tube.
3. Place the swab specimen in the Extraction Tube. Squeeze the tube and twirl the swab 10 seconds, make sure the specimen release into the extraction buffer as much as possible. discard the swab and cover the extraction tube with dropper.
4. Add 2-3 full drops of solution to the specimen well (S) and then start the timer.
5. Read the result at 15 minutes. Do not interpret the result after 15 minutes.
Note: Very low concentrations of Flu A antigen might result in a weak line appearing in the test line regions after an extended period of time; therefore, do not read results after 15 minutes.
Product category: Diagnostic rapid tests
Virus Sampling Tube and Swab VTM UTM
Virus Sampling Tube and Swab is suitable for the collection,transportion and storage of various types of virus samples such as Covid-19,influenza virus,bird flu,hand-foot-mouth disease,leprosy,etc.
Charateristic:
Specification:
Non inactivated or inactivated(3ml preservation)
10ml Tube+Nylon flocking swab,30Kits/box
5ml Tube+Nylon flocking swab,40Kits/box
Storage and Validity:Store at 2-30℃ for 12 months
Charateristic:
- High security
- Stable nucleic
- Easy operation and wide application
Specification:
Non inactivated or inactivated(3ml preservation)
10ml Tube+Nylon flocking swab,30Kits/box
5ml Tube+Nylon flocking swab,40Kits/box
Storage and Validity:Store at 2-30℃ for 12 months
Product category: Diagnostic rapid tests
Dengue IgG IgM/NS1 Combo Rapid Test Kit
The Dengue IgG/IgM/NS1 Combo Rapid Test Device is a lateral flow chromatographic immunoassay for the qualitative detection of dengue IgG/ IgM and virus antigen (Dengue Ag) in human whole blood, serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with Dengue viruses. Any reactive specimen with the Dengue
IgG/IgM/NS1 Combo Rapid Test Device must be confirmed with alternative testing method(s) and clinical findings.
IgG/IgM/NS1 Combo Rapid Test Device must be confirmed with alternative testing method(s) and clinical findings.
Product category: Diagnostic rapid tests
Sexually Chlamydia Rapid Test Kit
The Chlamydia trachomatics antigen test kit is a rapid visual immunoassay for the qualitative detection of Chlamydia trachomatics in female endocervical swab, male urethral swab and urine specimens. This kit is intended for use as
an aid of diagnosis of Chlamydia trachomatics infection
an aid of diagnosis of Chlamydia trachomatics infection
Product category: Diagnostic rapid tests
Sexually HIV1/2 Rapid Test Kit
HIV 1/2 Rapid Test Kit is a lateral flow immunochromatographic assay for the qualitative detection of antibodies (IgG, IgM, IgA) to HIV-1 (including O) or HIV-2 virus in human serum, plasma or whole blood. It is intended to be used by professionals as a screening test and an aid in the diagnosis of infection with HIV-1 or HIV-2 viruses. Any reactive specimen with the HIV 1/2 Rapid Test Kit must be confirmed with alternative testing method(s).
Product category: Diagnostic rapid tests
Bi-state Blood Culture Bottle for the qualitative detection of microorganisms
Introduction
Blood culture is one of the most important and critical procedures
performed in the microbiology laboratory. Since blood is normally sterile, the
isolation and identification of an organism has great diagnostic significance.
Mostly used to diagnosis microorganisms specially for some fastidious organisms
such as Haemophilus influenzae,neisseria meningitides,streptococcus pneumonia,bacterium
burgeri,actinobacillus,cardiobacterium hominis,kingella. It is important to diagnosis infection bacteremia and septicemia.
Intend to use
Ready to use culture medium based assay for the qualitative detection of
microorganisms in body fluids like blood, ascites, cerebrospinal fluid, etc,
offering isolated strains to carry out susceptibility tests.
Kit Components
Peptone, beef extract,hemin,yeast,SPS,autoclaving
Procedure
Read the entire procedure carefully prior to testing.
1. Check if the bottle is contaminated or broken.
2. Prepare and label the appropriate blood culture bottle
3. Do not unscrew cap. Remove the plastic top of the screw cap on
the blood culture bottle.
4. Disinfect the visible part of the rubber plug with iodine or ethyl
alcohol (70%) and allow drying.
5. Collect approximately 5-10 ml of adult patients’ blood , or 1-5 ml of infant
patients’ blood
6. Inject blood, ascites or cerebrospinal fluid into the culture bottle, after being
collected with aseptic operations. Then disinfect the rubber plug again and replace
the plastic top.
7. After the inoculation, lean the bottle several times, and incubate it,erectly
at (36±1) ℃ for 24 hours.
Interpretation of Result
1. Report the positive results if turbidity in the culture broth, hemolysis of
blood corpuscles, air bubbles or colonies is observed. Carry out
susceptibility tests and strain identification on positive samples.
2. Soak agar state into broth every day and keep on incubating the bottle
erectly if those phenomena do not occur, until the 7th day.
3. If the above mentioned phenomena still do not occur after 7 days of
culturing, report a negative result after confirm with microscopy and blind
passage.
Blood culture is one of the most important and critical procedures
performed in the microbiology laboratory. Since blood is normally sterile, the
isolation and identification of an organism has great diagnostic significance.
Mostly used to diagnosis microorganisms specially for some fastidious organisms
such as Haemophilus influenzae,neisseria meningitides,streptococcus pneumonia,bacterium
burgeri,actinobacillus,cardiobacterium hominis,kingella. It is important to diagnosis infection bacteremia and septicemia.
Intend to use
Ready to use culture medium based assay for the qualitative detection of
microorganisms in body fluids like blood, ascites, cerebrospinal fluid, etc,
offering isolated strains to carry out susceptibility tests.
Kit Components
Peptone, beef extract,hemin,yeast,SPS,autoclaving
Procedure
Read the entire procedure carefully prior to testing.
1. Check if the bottle is contaminated or broken.
2. Prepare and label the appropriate blood culture bottle
3. Do not unscrew cap. Remove the plastic top of the screw cap on
the blood culture bottle.
4. Disinfect the visible part of the rubber plug with iodine or ethyl
alcohol (70%) and allow drying.
5. Collect approximately 5-10 ml of adult patients’ blood , or 1-5 ml of infant
patients’ blood
6. Inject blood, ascites or cerebrospinal fluid into the culture bottle, after being
collected with aseptic operations. Then disinfect the rubber plug again and replace
the plastic top.
7. After the inoculation, lean the bottle several times, and incubate it,erectly
at (36±1) ℃ for 24 hours.
Interpretation of Result
1. Report the positive results if turbidity in the culture broth, hemolysis of
blood corpuscles, air bubbles or colonies is observed. Carry out
susceptibility tests and strain identification on positive samples.
2. Soak agar state into broth every day and keep on incubating the bottle
erectly if those phenomena do not occur, until the 7th day.
3. If the above mentioned phenomena still do not occur after 7 days of
culturing, report a negative result after confirm with microscopy and blind
passage.
Product category: Diagnostic rapid tests
ToRCH Toxo/Rubella/CMV/HSV1/2 IgG/IgM Rapid Test Kit
The ToRCH Toxo/Rubella/CMV/HSV1/2 IgG/IgM Rapid Test Cassette is a lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Toxoplasma gondii (Toxo), Rubella virus (Rubella), Cytomegalovirus (CMV) and Herpes simplex virus 1/2 (HSV 1/2) in human Serum or Plasma. It provides an aid in the diagnosis of infection with ToRCH
Product category: Diagnostic rapid tests
HCV Rapid Test Kit
The HCV Rapid Test is a double antigen lateral flow chromatographic immunoassay for the
qualitative detection of anti‐hepatitis C virus antibodies (IgG, IgM, IgA) in human serum,
plasma or whole blood. It is intended to be used as a screening test and as an aid in the
diagnosis of infection with HCV. Any reactive specimen with the HCV
qualitative detection of anti‐hepatitis C virus antibodies (IgG, IgM, IgA) in human serum,
plasma or whole blood. It is intended to be used as a screening test and as an aid in the
diagnosis of infection with HCV. Any reactive specimen with the HCV
Product category: Diagnostic rapid tests
iGFBP-1 PROM Rapid Test Kit
The Insulin-like growth factor-binding protein 1 (iGFBP-1) rapid test (vaginal secretion) is
a visually interpreted, qualitative immunochromatographic test device for detection of
iGFBP-1 in vaginal secretions during pregnancy, which is a major protein marker of the
amniotic fluid in a vaginal sample. The test is intended for professional use to help diagnose
the rupture of fetal membranes (ROM) in pregnant women.
a visually interpreted, qualitative immunochromatographic test device for detection of
iGFBP-1 in vaginal secretions during pregnancy, which is a major protein marker of the
amniotic fluid in a vaginal sample. The test is intended for professional use to help diagnose
the rupture of fetal membranes (ROM) in pregnant women.
Product category: Diagnostic rapid tests
Malaria Pf/Pan Antigen Rapid Test Kit
The Malaria Pf/Pan Rapid Test Device is a rapid chromatographic immunoassay for the qualitative
detection of circulating antigens of Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale,
Plasmodiummalariae in whole blood
detection of circulating antigens of Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale,
Plasmodiummalariae in whole blood
Product category: Diagnostic rapid tests
Helicobacter Pylori HP Ag Self Rapid Test Kit
The Helicobacter-Pylori antigen rapid test device (stool) is a rapid visual immunoassay for the qualitative detection of helicobacter pylori antigen in human stool specimens. This device is used as an aid in the diagnosis of H. pylori infection.
Product category: Diagnostic rapid tests
10 parameter Urinalysis reagent test strip
Summary
Urinalysis Reagent Strips are made for urinalysis of both qualita tive and semi-quantitative, which are in vitro reagent for diagnos tics. It tests Leukocytes, Nitrite, Urobili nogen, Protein, pH, Blood,Specific Gravity,Ascorbic Acid, Ketone, Bilirubin , Glucose, Microalbumin in urine. Please refer to the out-side box and bottle label for the specific test parameters of the product you are using Please read this direction carefully before using.The results on the strips can be read visually and instrumentally.
Specification
100strips/barrel
Specimen Collection and Preparation
Use only clean dry container to collect urine and should be shocked before testing
and test it within 2 hours. Any operations must be in the clean environment
Test Procedure
1.Remove one strip from the bottle and replace the cap immediately
2.Immerse the reagent area of the strip in the urine specimen and take it out quickly
3.Wipe off excess urine against the rim of the specimen container.
4.Read the test results carefully within 60 seconds in a good light and with the test area held near the appropriate color chart on the bottle label. Changes in color that appear only along the edges of the test pads or after moving than 2 minutes have passed are of no diagnostic significance. Results with leukocytes test portion can be read within 120 seconds.
If reading instrumentally, carefully follow the directions given in the appropriate instrument operating manual
Urinalysis Reagent Strips are made for urinalysis of both qualita tive and semi-quantitative, which are in vitro reagent for diagnos tics. It tests Leukocytes, Nitrite, Urobili nogen, Protein, pH, Blood,Specific Gravity,Ascorbic Acid, Ketone, Bilirubin , Glucose, Microalbumin in urine. Please refer to the out-side box and bottle label for the specific test parameters of the product you are using Please read this direction carefully before using.The results on the strips can be read visually and instrumentally.
Specification
100strips/barrel
Specimen Collection and Preparation
Use only clean dry container to collect urine and should be shocked before testing
and test it within 2 hours. Any operations must be in the clean environment
Test Procedure
1.Remove one strip from the bottle and replace the cap immediately
2.Immerse the reagent area of the strip in the urine specimen and take it out quickly
3.Wipe off excess urine against the rim of the specimen container.
4.Read the test results carefully within 60 seconds in a good light and with the test area held near the appropriate color chart on the bottle label. Changes in color that appear only along the edges of the test pads or after moving than 2 minutes have passed are of no diagnostic significance. Results with leukocytes test portion can be read within 120 seconds.
If reading instrumentally, carefully follow the directions given in the appropriate instrument operating manual
Product category: Diagnostic rapid tests
Mycoplasma Identification Susceptibility Test Kit (Freeze-dried)
Mycoplasma Identification Susceptibility Test Kit (Freeze-dried)
1.Human Mycoplasma culture media .
2.High sensitivity and specificity
3.Precision,accuracy,stability
4. Human Mycoplasma test kit
PACKAGE SPECIFICATION
20 tests/kit.
APPLICATION
For the isolation, identification, enumeration and antibiotic susceptibility tests of urogenital tract
Ureaplasma Urealyticum (UU) and Mycoplasma Hominis (MH) in one step.
TEST PRINCIPLE
The test kit consists of freeze-dried type culture broth and susceptibility test boards. The broth contains peptone, yeast extract, serum, growth factors and other nutrients, and urea, arginine as well. The alkaline material produced by urea, arginine decomposition causes the broth pH value rise, so the broth color changes from yellow to red. The broth has antibacterial agent which inhibits the growth of bacteria and fungi. The test board’s wells are used for control test and the UU and MH identification, enumeration and susceptibility tests.
MAIN COMPONENTS
1) Urea-arginine broth (freeze-dried): 20 vials
2) Susceptibility test board: 20 pcs
3) Sterile pipette tip: 20 pcs
4) Sterile paraffin oil: 2 bottles
5) Sterile diluting liquid: 2 bottles
6) Instruction: 1 pcs
7) Report booklet: 1 pcs
STORAGE AND PERIOD OF VALIDITY
Stored at 2-8°C ; 12 months.
SUSCEPTIBILITY FOR TEST
1) 10-antibiotic: Doxycycline (DOX), Minomyclin (MIN), Ciprofloxacin (CPF), Ofloxacin (OFL), Sparfloxacin (SPA), Roxithromycin (ROX), Azithromycin (AZI), Clarithromycin (CLA), Josamycin (JOS), Spectinomycin (SPE).
1.Human Mycoplasma culture media .
2.High sensitivity and specificity
3.Precision,accuracy,stability
4. Human Mycoplasma test kit
PACKAGE SPECIFICATION
20 tests/kit.
APPLICATION
For the isolation, identification, enumeration and antibiotic susceptibility tests of urogenital tract
Ureaplasma Urealyticum (UU) and Mycoplasma Hominis (MH) in one step.
TEST PRINCIPLE
The test kit consists of freeze-dried type culture broth and susceptibility test boards. The broth contains peptone, yeast extract, serum, growth factors and other nutrients, and urea, arginine as well. The alkaline material produced by urea, arginine decomposition causes the broth pH value rise, so the broth color changes from yellow to red. The broth has antibacterial agent which inhibits the growth of bacteria and fungi. The test board’s wells are used for control test and the UU and MH identification, enumeration and susceptibility tests.
MAIN COMPONENTS
1) Urea-arginine broth (freeze-dried): 20 vials
2) Susceptibility test board: 20 pcs
3) Sterile pipette tip: 20 pcs
4) Sterile paraffin oil: 2 bottles
5) Sterile diluting liquid: 2 bottles
6) Instruction: 1 pcs
7) Report booklet: 1 pcs
STORAGE AND PERIOD OF VALIDITY
Stored at 2-8°C ; 12 months.
SUSCEPTIBILITY FOR TEST
1) 10-antibiotic: Doxycycline (DOX), Minomyclin (MIN), Ciprofloxacin (CPF), Ofloxacin (OFL), Sparfloxacin (SPA), Roxithromycin (ROX), Azithromycin (AZI), Clarithromycin (CLA), Josamycin (JOS), Spectinomycin (SPE).
Product category: Diagnostic rapid tests
Encode Produce more than 115 items of in vitro diagnostic tests
Welcome inquiry for Encode Diagnostic Rapid Tests and Microbiological Tests!
Microbiological Culture Series
M0005 Mycoplasma Culture Medium
M0010 TB Drug Susceptibility Test Kit
M0019 Bi-phase blood culture bottle
M0020 Anaerobic blood culture bottle
Infectious Disease Rapid Tests
COVID-19 antibody,Covid-19 antigen,Tube and Swab,M.Tuberculosis,Helicobacter Pylori
Enteroviurs,Coxsackievirus,Entero/Coxsackie
Rota/Adenovirus,Rotavirus Group A,Adenovirus
HbsAg,HbsAb,HCV
Malaria,TORcH,Strep A,Dengue
Chagas,Chikungunya,Filariasis,Typhoid,S. typhoid,S. typhoid/ S. Para typhi,Toxoplasma
HAV,Leishmania,Brucellosis,Vitamin D,Leptospira,Zika IgG/IgM
Respiratory Diseases Tests
M.Pneumonia,C.Pneumonia,HPIVS,Influenza,RSV
Cholera O1
Cardiac Markers Tests
CKMB,MYO,TRO,CMC,hs-CRP,CRP,D-DIMER,PCT,H-FABP
Tumor Markers Tests
FOB,TF,Hb + Tf combo,PSA,CEA,AFP,Albumin
Fertility Test
HCG,i-GFBP,FFN,IGFBP+FFN
Sexually Transmitted Disease Tests
Neisseria Gonorrhea, Chlamydia Trachomatis,Gonorrhea +Chlamyida Combo Test
Bacterial Vaginosis,Syphilis,HIV 1/2,HIV 1+O/2,HSV-2,Rubella
Drugs of Abuse Tests (Strip,Cassette, Muliti-Dip, Muliti-Panel, Urine Cup are Available)
K2/AMP/BAR/BZO/BUP/COC/COT/MDMA/EDDP/FYL/KET/THC/MTD/MET/MQL/MOP/OPI/OXY/PCP/PPX/TCA/TML
Microbiological Culture Series
M0005 Mycoplasma Culture Medium
M0010 TB Drug Susceptibility Test Kit
M0019 Bi-phase blood culture bottle
M0020 Anaerobic blood culture bottle
Infectious Disease Rapid Tests
COVID-19 antibody,Covid-19 antigen,Tube and Swab,M.Tuberculosis,Helicobacter Pylori
Enteroviurs,Coxsackievirus,Entero/Coxsackie
Rota/Adenovirus,Rotavirus Group A,Adenovirus
HbsAg,HbsAb,HCV
Malaria,TORcH,Strep A,Dengue
Chagas,Chikungunya,Filariasis,Typhoid,S. typhoid,S. typhoid/ S. Para typhi,Toxoplasma
HAV,Leishmania,Brucellosis,Vitamin D,Leptospira,Zika IgG/IgM
Respiratory Diseases Tests
M.Pneumonia,C.Pneumonia,HPIVS,Influenza,RSV
Cholera O1
Cardiac Markers Tests
CKMB,MYO,TRO,CMC,hs-CRP,CRP,D-DIMER,PCT,H-FABP
Tumor Markers Tests
FOB,TF,Hb + Tf combo,PSA,CEA,AFP,Albumin
Fertility Test
HCG,i-GFBP,FFN,IGFBP+FFN
Sexually Transmitted Disease Tests
Neisseria Gonorrhea, Chlamydia Trachomatis,Gonorrhea +Chlamyida Combo Test
Bacterial Vaginosis,Syphilis,HIV 1/2,HIV 1+O/2,HSV-2,Rubella
Drugs of Abuse Tests (Strip,Cassette, Muliti-Dip, Muliti-Panel, Urine Cup are Available)
K2/AMP/BAR/BZO/BUP/COC/COT/MDMA/EDDP/FYL/KET/THC/MTD/MET/MQL/MOP/OPI/OXY/PCP/PPX/TCA/TML
About us
Company details
Zhuhai Encode Medical Engineering Co., Ltd (Hereinafter referred to Encode) was established in 1994,as one of the earliest and largest manufacturer of in-vitro diagnostic field in China. Encode specializes in R&D, production and distribution of in-vitro diagnostic products. As a hi-tech and innovative enterprise, we have researched and developed series of microbiological diagnostic products and immunology diagnostic rapid test, which are used for diagnosis of Infection Diseases, Cardiac Markers, Tumor Markers, Fertility test, Drug of Abuse and Transmitted disease. The Product has approved by CFDA, CE, ISO13485 and ISO9001.
In order to fight for Covid-19,Encode produce more than 9,000,000tests Covid-19 IgG/IgM Rapid Test since
February,the quality is highly recognized from customers and Covid-19 Antigen Rapid Test with 94% clinical sensitivity ,both of antibody test and antigen test with CE and ISO approved.
In order to fight for Covid-19,Encode produce more than 9,000,000tests Covid-19 IgG/IgM Rapid Test since
February,the quality is highly recognized from customers and Covid-19 Antigen Rapid Test with 94% clinical sensitivity ,both of antibody test and antigen test with CE and ISO approved.
Company data
Sales volume> 500 Mio US $
Export content> 75%
Number of employees100-499
Foundation1994
Area of business- Laboratory equipment
- Diagnostics
- Medical Services and Publications