← Back to catalogue

Latex Grouping Reagent C

FDA UDI

Class I (US FDA UDI)

by Oxoid Limited

Identity

Trade Name
Latex Grouping Reagent C FDA UDI
Generic Name
Beta-haemolytic Streptococcus serological grouping IVD, reagent FDA UDI
Model / Reference
DR0588G FDA UDI

Identifiers

Primary DI / UDI-DI
05032384013067 FDA UDI
FDA Product Code
GTZ FDA UDI
GMDN Term
Beta-haemolytic Streptococcus serological grouping IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3740 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: Beta-haemolytic Streptococcus serological grouping IVD, reagent

Latex Grouping Reagent C by Oxoid Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Beta-haemolytic Streptococcus serological grouping IVD, reagent.

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

Manufacturer
Oxoid Limited

Sources (1)

  • FDA UDI f1f50a01-5963-4fda-9478-d4d3c99cfb5e 32 fields · synced Jun 8, 2026