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Antiserum to Human C Reactive Protein

FDA UDI

Class II (US FDA UDI)

by Kent Laboratories, Inc.

Identity

Trade Name
Antiserum to Human C Reactive Protein FDA UDI
Generic Name
C-reactive protein (CRP) IVD, kit, precipitation/immunodiffusion FDA UDI
Device Name
goat antiserum to human C Reactive Protein FDA UDI
Model / Reference
1 FDA UDI
Description
goat antiserum to human C Reactive Protein FDA UDI

Identifiers

Catalog Number
134002 FDA UDI
Primary DI / UDI-DI
B1761340 FDA UDI
FDA Product Code
DCK 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

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

Yes

FDA UDI

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

Antiserum to Human C Reactive Protein by Kent 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

Manufacturer
Kent Laboratories, Inc.

Sources (1)

  • FDA UDI db46ec88-4007-456f-80b4-93dd892c59a2 34 fields · synced May 30, 2026