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MAY-GRÜNWALD roztok

EUDAMED

Class A (EU MDR)

Ref 21060

by Ing. Petr Švec - PENTA s.r.o.

Identity

Trade Name
MAY-GRÜNWALD roztok EUDAMED
Device Name
MAY-GRÜNWALD roztok EUDAMED
Model / Reference
21060 EUDAMED

Identifiers

Primary DI / UDI-DI
08595142233512 EUDAMED
Basic UDI-DI
85951422210606T EUDAMED
Direct Marketing DI
08595142233512 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

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

MAY-GRÜNWALD 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 0043773c-9206-4a2c-8851-ebde06e2d8a9 61 fields · synced Jul 10, 2026