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DIASTAT anti-Cardiolipin IgM

FDA UDI

Class II (US FDA UDI)

by Euro-Diagnostica AB

Identity

Trade Name
DIASTAT anti-Cardiolipin IgM FDA UDI
Generic Name
Anticardiolipin antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
FCAR100M FDA UDI

Identifiers

Catalog Number
FCAR100M FDA UDI
Primary DI / UDI-DI
07340058410233 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

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

DIASTAT anti-Cardiolipin IgM by Euro-Diagnostica AB — 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

Manufacturer
Euro-Diagnostica AB

Sources (1)

  • FDA UDI f3e79ed2-2125-40b0-831b-cf0e4ad92faa 33 fields · synced Jun 8, 2026