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EDIA anti-CCP

FDA UDI

Class II (US FDA UDI)

by Euro-Diagnostica AB

Identity

Trade Name
EDIA anti-CCP FDA UDI
Generic Name
Cyclic citrullinated peptide antibody (anti-CCP) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
FCCP100 FDA UDI

Identifiers

Catalog Number
FCCP100 FDA UDI
Primary DI / UDI-DI
07340058410615 FDA UDI
FDA Product Code
NHX FDA UDI
GMDN Term
Cyclic citrullinated peptide antibody (anti-CCP) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5775 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

Yes

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: Cyclic citrullinated peptide antibody (anti-CCP) IVD, kit, enzyme immunoassay (EIA)

EDIA anti-CCP by Euro-Diagnostica AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cyclic citrullinated peptide antibody (anti-CCP) IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Euro-Diagnostica AB

Sources (1)

  • FDA UDI e9fad5cf-58c7-4334-a776-97e16dc6cbb7 33 fields · synced Jun 8, 2026