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Urinal femme

EUDAMED

Class I (EU MDR)

Ref HEXUGBF25Model FN-UB0101010102

by Finess Healthcare Group Co., Ltd

Identity

Trade Name
Urinal femme EUDAMED
Device Name
Urine Bottle EUDAMED
Model / Reference
FN-UB0101010102 EUDAMED
HEXUGBF25 EUDAMED

Identifiers

Primary DI / UDI-DI
06978486830371 EUDAMED
Basic UDI-DI
697391169UB0101GK EUDAMED
EMDN Code
A06030399 URINE COLLECTION SYSTEMS - OTHER 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

Urinal femme 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 3dbdc873-9b5d-4586-a924-1a1f2d3721d0 61 fields · synced Sep 17, 2026