Address: STREP A OIA MAX Laboratory Procedure Test Principle The STREP A OIA MAX test involves the acid extraction from the throat swab specimen of a carbohydrate.

 

BioStar OIA RSV Laboratory Procedure Test Principle The OIA RSV test involves the extraction and detection of protein antigens unique to RSV nucleoprotein and fusion protein. The Optical.

 

BioStar OIA FLU A/B Laboratory Procedure Test Principle The BioStar OIA FLU A/B assay is an Optical ImmunoAssay OIA test for the qualitative, rapid detection of influenza A and B viral antigen.

 

BioStar OIA GC Laboratory Procedure Test Principle The BioStar® OIA GC test involves the extraction and detection of an antigen unique to N. gonorrhoeae. The Optical ImmunoAssay technology.

 

Address BioStar® OIA® STREP B LABORATORY PROCEDURE Test Principle The OIA STREP B test involves the extraction of a carbohydrate antigen unique to Group.

 

Address: BioStar® OIA® CHLAMYDIA Laboratory Procedure Test Principle The BioStar OIA CHLAMYDIA test involves the extraction of a antigen unique to Chlamydia.

 

Address BioStar® OIA® STREP B LABORATORY PROCEDURE Test Principle The OIA STREP B test involves the extraction of a carbohydrate antigen unique to Group.

 

Address: BioStar OIA SHIGATOX Laboratory Procedure Test Principle The BioStar® OIA® SHIGATOX assay is an Optical Immunoassay OIA test for the qualitative, rapid.

 

ThyroTest® TSH Laboratory Procedure Test Principle The ThyroTest one-step, rapid TSH assay for hypothyroidism screening in adults is a lateral flow chromatographic immunoassay.

 

ThyroTest® TSH Laboratory Procedure Test Principle The ThyroTest one-step, rapid TSH assay for hypothyroidism screening in adults is a lateral flow chromatographic immunoassay.

 

Procedure: Activated Clotting Time ACT Test Hemochron® Signature Hemochron Signature Elite® Approved by Date _______________ Created by Date Reviewed.

 

Citrate Activated Partial Thromboplastin Time Testing APTT Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date.

 

Activated Clotting Time Low Range Testing ACT-LR Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date Reviewed.

 

Prothrombin Time with INR PT/INR Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date Reviewed by Date Reviewed.

 

Citrate Activated Partial Thromboplastin Time Testing APTT Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date.

 

Prothrombin Time with INR PT/INR Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date Reviewed by Date Reviewed.

 

Activated Partial Thromboplastin Time Testing APTT Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date Reviewed.

 

Citrate Activated Partial Thromboplastin Time Testing APTT Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date.

 

Citrate Activated Partial Thromboplastin Time Testing APTT Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date.

 

Prothrombin Time with INR PT/INR Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date Reviewed by Date Reviewed.

 

Activated Clotting Time Low Range Testing ACT-LR Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date Reviewed.

 

Procedure: Activated Clotting Time ACT Test Hemochron® Signature Hemochron Signature Elite® Approved by Date _______________ Created by Date Reviewed.

 

Procedure: Activated Clotting Time ACT Test Hemochron® Signature Hemochron Signature Elite® Approved by Date _______________ Created by Date Reviewed.

 

Citrate Activated Partial Thromboplastin Time Testing APTT Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date.

 

Activated Clotting Time Low Range Testing ACT-LR Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date Reviewed.

 

Activated Partial Thromboplastin Time Testing APTT Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date Reviewed.

 

Prothrombin Time with INR PT/INR Hemochron® Signature Hemochron Signature Elite® Approved by Date Created by Date Reviewed by Date Reviewed.

 

Hemochron® Response System Clinical and Laboratory Standards Institute CLSI Formatted Procedure Approved by Date Created by Date Reviewed by Date.

 

Address: BioStar Acceava Mono Test Laboratory Procedure The Acceava Mono test uses color dipstick technology with bovine.

 

Address: BioStar Acceava hCG Basic II Test Laboratory Procedure Test Principle The BioStar® Acceava® hCG Basic II test is a rapid chromatographic immunoassay.

 

Inverness Medical Clearview ULTRA FOB Test Laboratory Procedure Test Principle The Clearview ULTRA FOB Test is an in vitro immunoassay for the rapid, qualitative.

 

Address: BioStar Acceava hCG Combo II Waived Test Laboratory Procedure Test Principle The BioStar Acceava hCG Combo II Test is a rapid chromatographic.

 

Binax NOW RSV Laboratory Procedure Test Principle The Binax NOW RSV Test is an membrane assay used to detect RSV fusion protein antigen in nasal wash.

 

Address: Specimen A. Specimen: Acceptable: Fingerstick and Venous Whole Blood Unacceptable: Other specimens collected from other sources B: Specimen.

 

Address: Clearview hCG Urine Cassette Test Laboratory Procedure Test Principle The Clearview® hCG Urine Test is a rapid chromatographic immunoassay for the qualitative.

 

Address: Clearview Strep A Exact II Dipstick Test Laboratory Procedure Test Principle The Clearview Strep A Exact II dipstick is a qualitative, lateral.

 

Address: BioStar Acceava hCG Urine II Test Laboratory Procedure Test Principle The BioStar Acceava hCG Urine II Test is a rapid chromatographic immunoassay.

 

Address: BioStar Acceava H. pylori Waived Test Laboratory Procedure I. Test Principle The BioStar® Acceava H. pylori Test utilizes solid-phase.

 

Address: Clearview H. pylori Test Laboratory Procedure Test Principle The Clearview H. pylori test is a rapid chromatographic immunoassay for the qualitative detection.

 

Address: BioStar Acceava H. pylori Test Laboratory Procedure I. Test Principle The Acceava H. pylori Anti-H. pylori IgA/IgG/IgM Antibody Test.

 

Address: TOX A/B QUIK CHEK Laboratory Procedure Test Principle The TOX A/B QUIK CHEK uses antibodies specific for toxins A and B of C. difficile. The device contains.

 

Address: Clearview® Mono Laboratory Procedure Test Principle The Clearview® Mono test is a rapid chromatographic immunoassay for the qualitative detection of Infectious.

 

Address: Binax NOW Legionella Urinary Antigen Laboratory Procedure Test Principle The Binax NOW Legionella Urinary Antigen Test is an membrane assay.

 

Clearview Simplify D-dimer Laboratory Procedure Test Principle The Clearview Simplify D-dimer test uses the D-dimer specific murine monoclonal.

 

Address: Clearview Strep A Exact II Cassette Test Laboratory Procedure Test Principle The Clearview Strep A Exact II Cassette is a qualitative, lateral.

 

Binax NOW Streptococcus pneumoniae Laboratory Procedure Test Principle The Binax NOW Streptococcus pneumoniae Test is an membrane assay used to detect pneumococcal.

 

Address: Clearview H. pylori Test Laboratory Procedure Test Principle The Clearview® H. pylori test is a rapid chromatographic immunoassay for the qualitative detection.

 

Address: Clearview® hCG Combo II Laboratory Procedure Test Principle The Clearview hCG Combo II test is a rapid chromatographic immunoassay for the qualitative detection of human.

 

Address: Specimen A. Specimen: Acceptable: Fingerstick and Venous Whole Blood Unacceptable: Other specimens collected from other sources B: Specimen.