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Immunex Crp®

FDA UDI

Class II (US FDA UDI)

by Alere North America, Llc

Identity

Trade Name
IMMUNEX CRP® FDA UDI
Generic Name
C-reactive protein (CRP) IVD, reagent FDA UDI
Model / Reference
71S2 FDA UDI

Identifiers

Primary DI / UDI-DI
10859035006016 FDA UDI
FDA Product Code
DCN FDA UDI
GMDN Term
C-reactive protein (CRP) IVD, reagent 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

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: C-reactive protein (CRP) IVD, reagent

Immunex Crp® by Alere North America, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as C-reactive protein (CRP) IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eff89075-acdb-416c-b817-5ccbc2ac0ea0 34 fields · synced May 31, 2026