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Arcobacter Broth

FDA UDI

Class I (US FDA UDI)

by Oxoid Limited

Identity

Trade Name
ARCOBACTER BROTH FDA UDI
Generic Name
Differential/selective broth culture medium IVD FDA UDI
Model / Reference
CM0965B FDA UDI

Identifiers

Primary DI / UDI-DI
05032384004911 FDA UDI
FDA Product Code
JSJ FDA UDI
GMDN Term
Differential/selective broth culture medium IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2360 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: Differential/selective broth culture medium IVD

Arcobacter Broth by Oxoid Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Differential/selective broth culture medium IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oxoid Limited

Sources (1)

  • FDA UDI 401c134a-a038-49b3-8d70-7bec6192e510 32 fields · synced Jun 1, 2026