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ProSpecT Campylobacter Microplate Assay 96 Tests

FDA UDI

Class I (US FDA UDI)

by Oxoid Limited

Identity

Trade Name
ProSpecT Campylobacter Microplate Assay 96 Tests FDA UDI
Generic Name
Multiple Campylobacter species antigen IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
R2476096 FDA UDI

Identifiers

Primary DI / UDI-DI
05032384519583 FDA UDI
FDA Product Code
LQP FDA UDI
GMDN Term
Multiple Campylobacter species antigen IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3110 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple Campylobacter species antigen IVD, kit, enzyme immunoassay (EIA)

ProSpecT Campylobacter Microplate Assay 96 Tests by Oxoid Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple Campylobacter species antigen IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oxoid Limited

Sources (1)

  • FDA UDI e8dd6b42-adb7-43db-b370-e5cc45e4f184 32 fields · synced Jun 6, 2026