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ELISA Cardiolipin IgM Test System

FDA UDI

by Zeus Scientific, Inc.

Identity

Trade Name
ELISA Cardiolipin IgM Test System FDA UDI
Generic Name
Anticardiolipin antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
The ZEUS ELISA Cardiolipin IgM Test System is an enzyme-linked immunosorbent assay (ELISA) designed for the semi-quantitative measurement of circulating IgM autoantibodies to Cardiolipin. FDA UDI
Model / Reference
2Z51051M FDA UDI
Description
The ZEUS ELISA Cardiolipin IgM Test System is an enzyme-linked immunosorbent assay (ELISA) designed for the semi-quantitative measurement of circulating IgM autoantibodies to Cardiolipin. FDA UDI

Identifiers

Catalog Number
2Z51051M FDA UDI
Primary DI / UDI-DI
00845533000321 FDA UDI
GMDN Term
Anticardiolipin antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

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

No

FDA UDI

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

ELISA Cardiolipin IgM Test System by Zeus Scientific, Inc. — 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 dcc8a6cc-199a-41b3-ab13-73bacc445313 35 fields · synced May 30, 2026