Nano-Ditech Corporation of Cranbury, NJ at MEDICA 2019 in Düsseldorf -- MEDICA - World Forum for Medicine
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Nano-Ditech Corporation

259 Prospect Plains Road, Building H, Building K, 08512 Cranbury, NJ
USA

This company is co-exhibitor of
Messe Düsseldorf North America

Hall map

MEDICA 2019 hall map (Hall 3): stand C46-3

Fairground map

MEDICA 2019 fairground map: Hall 3

Our range of products

Product categories

  • 03  Diagnostic Tests
  • 03.02  Immunochemistry testing, immunology testing
  • 03.02.02  Diagnostic rapid tests

Our products

Product category: Diagnostic rapid tests

Nano-CheckTM AMI Cardiac Test

Nano-CheckTM AMI Cardiac Test is a rapid immunoassay for the quantitative or qualitative determination of three keys cardiac markers in whole blood, plasma, or serum as an aid in early detection of Acute Myocardial Infarction (AMI) in the Emergency room and Physician’s office. The device provides quantitative / qualitative measurements of key cardiac markers (cTnI, CK-MB, and Myoglobin) simultaneously or separately.

Technology: Immunochromatography
Turn Around Time: 15 minutes
Sample Type: Whole Blood, Plasma, Serum
Volume of Sample Required: 80 μL
Measuring Range:

cTnI:0.1 ng/mL- 30 ng/mL
CK-MB: 2 ng/mL- 200 ng/mL
Myo: 20 ng/mL- 1,000 ng/mL
NT-proBNP: 30 pg/mL- 15,000 pg/mL
Storage: Room Temperature (2-30 ℃)
Shelf Life: 15 months
Package: 20 test cassettes / box
Box Contents: 20 test cassettes, 20 disposable Pipettes, 1 instruction Manual

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Product category: Diagnostic rapid tests

Nano-CheckTM PCT

Nano-CheckTMPCT test is used for the determination of PCT in whole blood, serum, or plasma specimens for patients who may have systemic or severe bacterial infection including bacterial pneumonia and bacterial meningitis. The test is used as an aid in the diagnosis of individuals suspected of sepsis.

Technology: Immunochromatography
Turn Around Time: 15 minutes
Sample Type: Whole Blood, Plasma, or Serum
Volume of Sample Required: 80 μl
Measuring Range: 0.1 ng/mL- 21 ng/mL
Storage: Room Temperature (2-30 ℃)
Shelf Life: 15 months
Package: 20 test cassettes / box
Box Contents: 20 test cassettes, 20 micro pipettes, 1 instruction manual

Catalogue No.: ND-CD7155

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Product category: Diagnostic rapid tests

Nano-CheckTM DAT

Drug of Abuse Test

Nano-CheckTMDAT is a One-step immunochromatography assay that detects the presence of any of 13 different illicit drugs in urine samples within 10 minutes. Nano-CheckTMDAT is the most comprehensive multidrug panel format in the DAT industry. The product is easy to use and can screen as many as 10 different drugs of abuse simultaneously.

Technology: Urine based Immunochromatography
Sample Type: Urine
Volume of Sample Required: 80 μL
Storage: Room Temperature (2-30 ℃)
Shelf Life: 15 months
Package: 25 test cassettes / box
Box Contents: 25 test cassettes, 25 disposable pipettes, 1 instruction manual

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Product category: Diagnostic rapid tests

Fluoro-CheckTM AMI cTnI Test

Fluoro-CheckTM AMI cTnI Test is a time resolved fluorescence immunoassay for the quantitative determination of Cardiac Troponin I (cTnI) in human whole blood, serum, or plasma specimen at detection limit concentration of 0.03 ng/ml as an aid in the diagnosis of acute myocardial infarction (AMI) and cardiac muscle damage. In conjunction with Fluoro-CheckerTM TRF reader, Fluoro-CheckTM AMI cTnI Test can monitor the rise and fall of cTnI.

Technology: Immunochromatography (Time Resolved Fluorescence)
Turn Around Time: 15 minutes
Sample Type: Whole Blood, Plasma, or Serum
Volume of Sample Required: 80 μL
Measuring Range: 0.03 ng/mL- 30 ng/mL
Storage: Room Temperature (2-30 ℃)
Shelf Life: 12 months
Package: 20 test cassettes / box
Box Contents: 20 test cassettes, 20 disposable pipettes, 1 instruction manual, 1 QR card

Catalog No.: ND-TF3151

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Product category: Diagnostic rapid tests

Fluoro-CheckTM PCT Test

Fluoro-CheckTM PCT test is a time resolved fluorescence immunoassay for the quantitative determination of PCT (Procalcitonin) level in human whole blood, serum or plasma specimens for patients who may have systemic or severe bacterial infection including bacterial pneumonia and bacterial meningitis.

Technology: Immunochromatography (Time Resolved Fluorescence)
Turn Around Time: 15 minutes
Sample Type: Whole Blood, Plasma, or Serum
Volume of Sample Required: 10 μL of Serum or Plasma, or 20 μL of Whole Blood (finger prick)
Measuring Range: 0.07 ng/mL- 30 ng/mL
Storage: Room Temperature (2-30 ℃)
Shelf Life: 12 months
Package: 20 test cassettes / box
Box Contents: 20 test cassettes, 20 micro pipettes, 1 instruction manual. 1QR card

Catalog No.: ND-TF3161

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About us

Company details

Founded in 2002, Nano-Ditech Corp specializes in the development and manufacture of high quality rapid immuno-diagnostic products to serve the point-of-care market place including medical professionals, physicians, clinical laboratories and hospitals. We focus on rapid POCT immunoassays for the detection of drugs of abuse, inflammation and cardiac markers in the emergency department. Nano-Ditech’s key workforce has extensive experience in the IVD industry and utilizes their experience to satisfy customer needs by ensuring the highest level of product quality.

Nano-Ditech's is proud to be among the few that have a track record for successfully developing test devices through the development of raw materials and obtaining US FDA and CE clearance. Nano-Ditech’s unique techniques have enabled us to rapidly develop all classes of monoclonal antibodies for each of the illicit drugs and cardiac disease markers to be specifically used for the rapid assay.

Nano-Ditech’s expert keep optimal quality control to provide a very high price/performance ratio of products.
Nano-Ditech also has developed a new generation of immunoassay device called Europium based TRF (Time Resolved Florescence) immunoassay. This single use diagnostic device will provide a new platform technology for the growing IVD market. The innovated technology will be further developed as a variety of POC diagnostic products through the collaboration of Nano-Ditech’s proprietary technologies or external partnering arrangements. In 2014, we successfully commercialized the technology with a unique TRF device reader and data management system. This diagnostic device system can be applied to various immunoassays used today requiring a highly sensitive and accurate standard.

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