← Back to catalogue

cobas Buffer Negative Control Kit

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
cobas Buffer Negative Control Kit FDA UDI
Generic Name
PCR/NAT negative control IVD FDA UDI
Model / Reference
09051953190 FDA UDI

Identifiers

Catalog Number
09051953190 FDA UDI
Primary DI / UDI-DI
00875197006926 FDA UDI
FDA Product Code
NSU FDA UDI
GMDN Term
PCR/NAT negative control IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.2570 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: PCR/NAT negative control IVD

cobas Buffer Negative Control Kit by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as PCR/NAT negative control IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 4869f3e5-0323-4e9a-9d82-67da2509b773 33 fields · synced May 30, 2026