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Hayem Roztok

EUDAMED

Class A (EU MDR)

Ref 14710

by Ing. Petr Švec - PENTA s.r.o.

Identity

Trade Name
HAYEM ROZTOK EUDAMED
Device Name
HAYEM ROZTOK EUDAMED
Model / Reference
14710 EUDAMED

Identifiers

Primary DI / UDI-DI
08595142233413 EUDAMED
Basic UDI-DI
85951422147107R EUDAMED
Direct Marketing DI
08595142233413 EUDAMED
EMDN Code
W01030199 HAEMATOLOGY REAGENTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Czechia 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

No

EUDAMED

Companion Diagnostics

Yes

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Hayem Roztok by Ing. Petr Švec - PENTA s.r.o. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CZ-MF-000035988

Sources (1)

  • EUDAMED 190faab1-08c4-490f-b994-526d01ad73af 61 fields · synced Jun 19, 2026