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ΑΛΚ.ΦΩΣΦΑΤΑΣΗ IFCC R1:8x50, R2 4x20 ml (ΗΙΤ)

EUDAMED

Class IVD General (EU MDR)

Ref 001517

by Biotechnological Applications Ltd

Identity

Trade Name
ΑΛΚ.ΦΩΣΦΑΤΑΣΗ IFCC R1:8x50, R2 4x20 ml (ΗΙΤ) EUDAMED
Device Name
ΑΛΚ.ΦΩΣΦΑΤΑΣΗ IFCC R1:8x50, R2 4x20 ml (ΗΙΤ) EUDAMED
Model / Reference
001517 EUDAMED

Identifiers

Primary DI / UDI-DI
05213003191483 EUDAMED
Basic UDI-DI
B-05213003191483 EUDAMED
EMDN Code
W01010105 ALKALINE PHOSPHATASE - TOTAL 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

ΑΛΚ.ΦΩΣΦΑΤΑΣΗ IFCC R1:8x50, R2 4x20 ml (ΗΙΤ) by Biotechnological Applications Ltd — 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

EUDAMED SRN
GR-MF-000033000

Sources (1)

  • EUDAMED 7897dadb-b398-412e-b9bd-4c6356ea6a75 61 fields · synced Jul 12, 2026