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Barberhøvel dobbel blå for engangsbruk

EUDAMED

Class I (EU MDR)

Ref 388994Model FN-RZ01

by Finess Healthcare Group Co., Ltd

Identity

Trade Name
Barberhøvel dobbel blå for engangsbruk EUDAMED
Device Name
Razor EUDAMED
Model / Reference
FN-RZ01 EUDAMED
388994 EUDAMED

Identifiers

Primary DI / UDI-DI
16978486830163 EUDAMED
Basic UDI-DI
697391169RZ01RH EUDAMED
EMDN Code
V010301 BLADES WITH SAFETY SYSTEMS, SINGLE-USE - NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Norway EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Barberhøvel dobbel blå for engangsbruk by Finess Healthcare Group Co., Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000004124
Authorised Representative
Zoustech S.L. ES-AR-000002008

Sources (1)

  • EUDAMED 0815563a-ec61-480a-bfd1-91ab5fdc84aa 61 fields · synced Jun 19, 2026