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GOT LIQUID R1:3x60, R2:1x45 ml

EUDAMED

Class IVD General (EU MDR)

Ref 001695

by Biotechnological Applications Ltd

Identity

Trade Name
GOT LIQUID R1:3x60, R2:1x45 ml EUDAMED
Device Name
GOT LIQUID R1:3x60, R2:1x45 ml EUDAMED
Model / Reference
001695 EUDAMED

Identifiers

Primary DI / UDI-DI
05213003192596 EUDAMED
Basic UDI-DI
B-05213003192596 EUDAMED
EMDN Code
W01010110 ASPARTATE AMINO-TRANSFERASE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Greece 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

GOT LIQUID R1:3x60, R2:1x45 ml by Biotechnological Applications Ltd — 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

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Manufacturer

EUDAMED SRN
GR-MF-000033000

Sources (1)

  • EUDAMED 1dfd3ca0-dc99-4b6d-9d29-ecfde88b0040 61 fields · synced Jun 18, 2026