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cobas® HBV is a quantitative nucleic acid test from Roche Diagnostics, listed for hepatitis B virus. Stated instrument compatibility: cobas® 5800, cobas® 6800, cobas® 8800. Registration status and availability vary by market.

Application: Bloodborne

Listing compiled from the manufacturer product page. Confirm registration status in the target market, sample type, and instrument compatibility before issuing an RFQ.

cobas® HBV (cobas® 4800) is a quantitative nucleic acid test from Roche Diagnostics, listed for hepatitis B virus. Stated instrument compatibility: cobas® 4800. Registration status and availability vary by market.

Application: Bloodborne

Listing compiled from the manufacturer product page. Confirm registration status in the target market, sample type, and instrument compatibility before issuing an RFQ.

cobas® HCV is a quantitative nucleic acid test from Roche Diagnostics, listed for hepatitis C virus. Stated instrument compatibility: cobas® 5800, cobas® 6800, cobas® 8800. Registration status and availability vary by market.

Application: Bloodborne

Listing compiled from the manufacturer product page. Confirm registration status in the target market, sample type, and instrument compatibility before issuing an RFQ.

cobas® HCV (cobas® 4800) is a quantitative nucleic acid test from Roche Diagnostics, listed for hepatitis C virus. Stated instrument compatibility: cobas® 4800. Registration status and availability vary by market.

Application: Bloodborne

Listing compiled from the manufacturer product page. Confirm registration status in the target market, sample type, and instrument compatibility before issuing an RFQ.

cobas® HCV GT is a nucleic acid test from Roche Diagnostics, listed for hepatitis C virus. Stated instrument compatibility: cobas® 4800. Registration status and availability vary by market.

Application: Bloodborne

Listing compiled from the manufacturer product page. Confirm registration status in the target market, sample type, and instrument compatibility before issuing an RFQ.

cobas® HIV-1 is a quantitative nucleic acid test from Roche Diagnostics, listed for HIV-1. Stated instrument compatibility: cobas® 5800, cobas® 6800, cobas® 8800. Registration status and availability vary by market.

Application: Bloodborne

Listing compiled from the manufacturer product page. Confirm registration status in the target market, sample type, and instrument compatibility before issuing an RFQ.

cobas® HIV-1 Test is a nucleic acid test from Roche Diagnostics, listed for HIV-1. Stated instrument compatibility: cobas® 4800. Registration status and availability vary by market.

Application: Bloodborne

Listing compiled from the manufacturer product page. Confirm registration status in the target market, sample type, and instrument compatibility before issuing an RFQ.

Elecsys® HCV Duo is a nucleic acid test from Roche Diagnostics, listed for hepatitis C virus. Registration status and availability vary by market.

Application: Bloodborne

Listing compiled from the manufacturer product page. Confirm registration status in the target market, sample type, and instrument compatibility before issuing an RFQ.

Elecsys® HIV combi PT is a nucleic acid test from Roche Diagnostics, listed for HIV-1. Registration status and availability vary by market.

Application: Bloodborne

Listing compiled from the manufacturer product page. Confirm registration status in the target market, sample type, and instrument compatibility before issuing an RFQ.

genesigPLEX qPCR Kit HBV/HCV/HIV1/HIV2 is a nucleic acid test from Novacyt (Primerdesign), listed for HIV-1. Registration status and availability vary by market.

Application: Bloodborne

Listing compiled from the manufacturer product page. Confirm registration status in the target market, sample type, and instrument compatibility before issuing an RFQ.

BCID Panel is catalogued from public product materials published by ZeptoMetrix Corporation. Availability: not published on this record. Regulatory status is manufacturer-reported and has not been independently verified. Confirm intended use, compatibility and local registration against official documentation before procurement.

Application: Bloodborne

Regulatory positioning is manufacturer-reported (ruo); verify scope and certificate details before procurement. Ask the manufacturer to confirm intended use, sample types and local registration status for your market.

LightMix® Modular HDV, Kit with reagents for 96 PCR reactions (20 μl) for detection of Hepatitis D Virus (HDV) RNA is catalogued from public product materials published by Roche Diagnostics. Availability: not published on this record. Regulatory status is manufacturer-reported and has not been independently verified. Confirm intended use, compatibility and local registration against official documentation before procurement.

Application: Bloodborne

Request confirmation of sample compatibility, regulatory position, service model, and supply continuity before issuing an RFQ.