PreciControl HIV Gen II 06924107162

GUDID 07613336183212

Roche Diagnostics GmbH

HIV1/HIV2 antigen/antibody IVD, control

• Primary Device ID: 07613336183212
• NIH Device Record Key: d02993bb-1894-4fc8-af7f-21c652d53223
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PreciControl HIV Gen II
• Version Model Number: 06924107162
• Catalog Number: 06924107162
• Company DUNS: 315028860
• Company Name: Roche Diagnostics GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613336183212 [Primary]

FDA Product Code

• QHM: Serology tests used for infectious disease screening of blood and plasma donations

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-02-27
• Device Publish Date: 2025-02-19

On-Brand Devices [PreciControl HIV Gen II]

• 04015630942503: 06924107160
• 07613336183212: 06924107162