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Quidel Inflammatory Test Kit InflammaDry® Dry Eye Test MMP-9 Tear Sample 20 Tests CLIA Waived - KT/20 - RPS-ID-20-U-KT

Quidel Inflammatory Test Kit InflammaDry® Dry Eye Test MMP-9 Tear Sample 20 Tests CLIA Waived - KT/20 - RPS-ID-20-U-KT

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Quidel Inflammatory Test Kit InflammaDry® Dry Eye Test MMP-9 Tear Sample 20 Tests CLIA Waived - K...

Item Id 1119893
MF Id# RPS-ID-20-U
Brand InflammaDry®
Manufacturer Quidel
Country of Origin United States
Application Inflammatory Test Kit
CLIA Classification CLIA Waived
CLIA Classified CLIA Waived
Contents 1 (20) Sample Collectors, (20) Test Cassettes, (20) Buffer Vial, Package Insert
Number of Tests 20 Tests
Product Dating McKesson Acceptable Dating: we will ship >= 90 days
Purchase Program Type Standard Purchase
Reading Type Visual Read
Sample Type Tear Sample
Specialty Immunoassay
Technology Direct Sampling Microfiltration Technology
Test Format Cassette Format
Test Name MMP-9
Test Type Dry Eye Test
Time to Results 10 Minute Results
UNSPSC Code 41116126

Features

  • Rapid, immunoassay test for the visual, qualitative, in vitro detection of elevated levels of the MMP-9 protein in human tears, from patients suspected of having dry eye
  • For in vitro diagnostic use only; for prescription use; single use only
  • Using direct sampling microfiltration technology, InflammaDry accurately identifies elevated levels of MMP-9 protein in tear fluid samples taken from the inside lining of the lower eyelid, the palpebral conjunctiva
  • InflammaDry is a disposable, low cost test, that requires no additional equipment to administer or interpret results
  • Using four simple steps, InflammaDry test results are achieved in just 10 minutes, aiding in the diagnosis of dry eye before the patient leaves the office
  • InflammaDry is the first and only, rapid result, in-office test that detects elevated levels of MMP-9, an inflammatory marker that is consistently elevated in the tears of patients with dry eye disease
  • A CLIA Certificate of Waiver is required to perform the test in a waived setting - This test is intended for prescription use at point-of-care sites
  • This product is required to be reported under California Proposition 65
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