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Anti-Cardiolipin IgG/IgM ELISA

FDA UDI

Class II (US FDA UDI)

by DRG International, Inc.

Identity

Trade Name
Anti-Cardiolipin IgG/IgM ELISA FDA UDI
Generic Name
Anticardiolipin antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Anti-Cardiolipin IgG / IgM ELISA is a test system for the quantitative measurement of IgG and IgM class autoantibodies against cardiolipin in human serum or plasma. FDA UDI
Model / Reference
EIA-3587 FDA UDI
Description
Anti-Cardiolipin IgG / IgM ELISA is a test system for the quantitative measurement of IgG and IgM class autoantibodies against cardiolipin in human serum or plasma. FDA UDI

Identifiers

Catalog Number
EIA-3587 FDA UDI
Primary DI / UDI-DI
00840239035875 FDA UDI
FDA Product Code
MID FDA UDI
GMDN Term
Anticardiolipin antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5660 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

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

Yes

FDA UDI

Category: Anticardiolipin antibody IVD, kit, enzyme immunoassay (EIA)

Anti-Cardiolipin IgG/IgM ELISA by DRG International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anticardiolipin antibody IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI debb06b8-688f-4a30-ac7b-82986f6032fd 36 fields · synced Jun 1, 2026