← Back to catalogue

Ast/Got

EUDAMED

Class IVD General (EU MDR)

Ref 4191/50

by Giesse Diagnostics Srl

Identity

Trade Name
AST/GOT EUDAMED
Device Name
AST/GOT EUDAMED
Model / Reference
4191/50 EUDAMED

Identifiers

Primary DI / UDI-DI
08053172970130 EUDAMED
Basic UDI-DI
B-08053172970130 EUDAMED
EMDN Code
W01010110 ASPARTATE AMINO-TRANSFERASE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Category: Total aspartate aminotransferase (AST) IVD, reagent

Ast/Got by Giesse Diagnostics Srl — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Total aspartate aminotransferase (AST) IVD, reagent.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
IT-MF-000039031

Sources (1)

  • EUDAMED f1b4b70a-2cf7-4740-90b5-a27028c6c2bd 61 fields · synced Jun 18, 2026