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Zkoumadlo Eosinový Roztok

EUDAMED

Class A (EU MDR)

Ref 41240

by Ing. Petr Švec - PENTA s.r.o.

Identity

Trade Name
ZKOUMADLO EOSINOVÝ ROZTOK EUDAMED
Device Name
ZKOUMADLO EOSINOVÝ ROZTOK EUDAMED
Model / Reference
41240 EUDAMED

Identifiers

Primary DI / UDI-DI
08595142247960 EUDAMED
Basic UDI-DI
85951422412407M EUDAMED
Direct Marketing DI
08595142247960 EUDAMED
EMDN Code
W01030708 STAIN SOLUTIONS (HISTOLOGY/CYTOLOGY) 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

Yes

EUDAMED

Companion Diagnostics

Yes

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Zkoumadlo Eosinový 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 e246df78-156d-4462-91cf-e8c7a774165a 61 fields · synced Aug 2, 2026