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GIEMSA-ROMANOWSKI roztok

EUDAMED

Class A (EU MDR)

Ref 14460-11000

by Ing. Petr Švec - PENTA s.r.o.

Identity

Trade Name
GIEMSA-ROMANOWSKI roztok EUDAMED
Device Name
GIEMSA-ROMANOWSKI roztok EUDAMED
Model / Reference
14460-11000 EUDAMED

Identifiers

Primary DI / UDI-DI
08595142233215 EUDAMED
Basic UDI-DI
85951422144607R EUDAMED
Direct Marketing DI
08595142233215 EUDAMED
EMDN Code
W0103010302 ROMANOWSKY STAINS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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

Yes

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

GIEMSA-ROMANOWSKI 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 2da6a350-574a-48f7-9cec-5e939717d3db 61 fields · synced Jul 15, 2026