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cobas liat SARS-CoV-2 & Influenza A/B v2 nucleic acid test

FDA UDI

Class II (US FDA UDI)

by Roche Molecular Systems, Inc.

Identity

Trade Name
cobas liat SARS-CoV-2 & Influenza A/B v2 nucleic acid test FDA UDI
Generic Name
Multiple-genus respiratory virus nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI
Model / Reference
09048634190 FDA UDI

Identifiers

Catalog Number
09048634190 FDA UDI
Primary DI / UDI-DI
00875197006285 FDA UDI
510(k) Number
K243400 FDA UDI
FDA Product Code
QOF FDA UDI
GMDN Term
Multiple-genus respiratory virus nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3981 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple-genus respiratory virus nucleic acid IVD, kit, nucleic acid technique (NAT)

cobas liat SARS-CoV-2 & Influenza A/B v2 nucleic acid test by Roche Molecular Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Multiple-genus respiratory virus nucleic acid IVD, kit, nucleic acid technique (NAT).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5554634b-0c10-4b0f-a48a-a20ab28861c5 34 fields · synced Jun 9, 2026