cobas® SARS-CoV-2 & Influenza A/B Quality Control Kit

Basic Information

• Brand Name: cobas® SARS-CoV-2 & Influenza A/B Quality Control Kit
• Primary DI: 00875197006377
• Version / Model: 09211128190
• Catalog Number: 09211128190
• Company Name: Roche Molecular Systems, Inc.
• Labeler DUNS: 071674100
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2026-02-24
• Public Version: 1
• Public Version Date: 2026-03-04
• Public Version Status: New
• Public Device Record Key: c9d7dc4e-efa3-4c94-924e-02b0357b1d0c

Device Characteristics

• Single Use: No
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
QOF	Multi-target respiratory specimen nucleic acid test including SARS-CoV-2 and other microbial agents	Microbiology	866.3981	2

GMDN Terms

Code	Name	Definition	Implantable	Status
47920	Multiple-genus respiratory virus nucleic acid IVD, control	A material which is used to verify the performance of an assay intended to be used for the qualitative and/or quantitative detection of nucleic acid from multiple virus genera associated with respiratory disease in a clinical specimen. Viruses intended to be detected may include respiratory syncytial virus (RSV), influenza viruses, parainfluenza viruses, human metapneumovirus, coronaviruses, enteroviruses, rhinoviruses and/or adenoviruses.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00875197006377	GS1

Premarket Submissions

Submission Number	Supplement Number
K223591	000