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cobas PCR Media

FDA UDI

Class I (US FDA UDI)

by Roche Molecular Systems, Inc.

Identity

Trade Name
cobas PCR Media FDA UDI
Generic Name
General specimen container IVD, additive/medium FDA UDI
Model / Reference
08261598190 FDA UDI

Identifiers

Catalog Number
08261598190 FDA UDI
Primary DI / UDI-DI
00875197006216 FDA UDI
FDA Product Code
PPM FDA UDI
GMDN Term
General specimen container IVD, additive/medium FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General specimen container IVD, additive/medium

cobas PCR Media by Roche Molecular Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen container IVD, additive/medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a5c84b67-55e9-4ef7-8a00-48c1dd3f86a4 33 fields · synced Jun 9, 2026