FDA Product Code, Supplement Authorization and FDA Listing Number are not required for BLA products.


Product Overview

FDA Product Code, Supplement Authorization and FDA Listing Number are not required for BLA products.
Procleix - Ultrio HCV D-Probes


Device Description

A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of human immunodeficiency virus 1 (HIV1) nucleic acid, Hepatitis C virus nucleic acid and/or Hepatitis B virus nucleic acid in a clinical specimen, using a nucleic acid technique (NAT).


Environmental Conditions

No Data Available


Device Sizes

No Data Available


Device Sterilization

Device Sterile: False

Sterilization Prior To Use: False

Sterilization Methods: No Data Available


Product Codes

No Data Available

Device Identifiers

Device Id: 15420045500648

Device Type: Primary

DeviceId Issuing Agency: GS1

Contains DI Number: N/A

Package Quantity: N/A

Package Discontinue Date: N/A

Package Status: N/A

Package Type: N/A


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