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Aim Crp Test

FDA UDI

Class II (US FDA UDI)

by Germaine Laboratories, Inc.

Identity

Trade Name
AIM CRP TEST FDA UDI
Generic Name
C-reactive protein (CRP) IVD, kit, precipitation/immunodiffusion FDA UDI
Device Name
Latex slide test for C Reactive Protein FDA UDI
Model / Reference
32100 FDA UDI
Description
Latex slide test for C Reactive Protein FDA UDI

Identifiers

Primary DI / UDI-DI
00695684321000 FDA UDI
FDA Product Code
DCN FDA UDI
GMDN Term
C-reactive protein (CRP) IVD, kit, precipitation/immunodiffusion FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5270 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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: C-reactive protein (CRP) IVD, kit, precipitation/immunodiffusion

Aim Crp Test by Germaine Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as C-reactive protein (CRP) IVD, kit, precipitation/immunodiffusion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7adc35a5-549e-4856-bc15-00a4b5b0c913 33 fields · synced May 30, 2026