← Back to catalogue

medimex Einmal-Rasierer, blau

EUDAMED

Class I (EU MDR)

Ref 8M50103002Model FN-RZ01

by Finess Healthcare Group Co., Ltd

Identity

Trade Name
medimex Einmal-Rasierer, blau EUDAMED
Device Name
Razor EUDAMED
Model / Reference
FN-RZ01 EUDAMED
8M50103002 EUDAMED

Identifiers

Primary DI / UDI-DI
06973911690742 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
Germany 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

medimex Einmal-Rasierer, blau 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 7a5ec8dd-3bc5-44c5-8317-58baed0b8ae9 61 fields · synced Jul 9, 2026