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Isletest™ IAA ELISA

EUDAMED

Class IVD General (EU MDR)

Ref 7011

by Biomerica, Inc.

Identity

Trade Name
Isletest™ IAA ELISA EUDAMED
Device Name
Isletest™ IAA ELISA EUDAMED
Model / Reference
7011 EUDAMED

Identifiers

Primary DI / UDI-DI
00083059070118 EUDAMED
Basic UDI-DI
B-00083059070118 EUDAMED
EMDN Code
W0102060104 INSULIN ANTIBODY EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Isletest™ IAA ELISA by Biomerica, Inc. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

Manufacturer
Biomerica, Inc.
EUDAMED SRN
US-MF-000015772
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED e19ea855-8dbc-47dd-b236-5cc13c8c694a 61 fields · synced Aug 1, 2026