Home / Clinical Laboratory / Test Kits / Rapid Test Kit / Rapid Test Kit InflammaDry® Dry Eye Test MMP-9 Tear Sample 20 TestsRPS-ID-20-U
Picture of Rapid Test Kit InflammaDry® Dry Eye Test MMP-9 Tear Sample 20 TestsRPS-ID-20-U

Rapid Test Kit InflammaDry® Dry Eye Test MMP-9 Tear Sample 20 TestsRPS-ID-20-U

Rapid-Test-Kit-InflammaDry®-Dry-Eye-Test-MMP-9-Tear-Sample-20-TestsRPS-ID-20-U

SKU #

#1119893

MPN #

RPS-ID-20-U

Brand

Quidel

Stock

In Stock

Quantity

100

Features

TEST KIT, INFLAMMADRY (20TEST/KT) D/S

$214.56 USD

Attribute Name Attribute Value
McKesson # 1119893
Manufacturer # RPS-ID-20-U
Brand InflammaDry®
Manufacturer Quidel
Application Rapid Test Kit
CLIA Classification CLIA Waived
Contents (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
Reading Type Visual Read
Sample Type Tear Sample
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

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  • 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