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Skinuvita Connector

EUDAMED

Class I (EU MDR)

Ref CONN

by Skinuvita GmbH

Identity

Device Name
Skinuvita Connector EUDAMED
Model / Reference
CONN EUDAMED

Identifiers

Primary DI / UDI-DI
04262439760023 EUDAMED
Basic UDI-DI
426243976CONNDN EUDAMED
Direct Marketing DI
04262439760023 EUDAMED
EMDN Code
Z12040280 GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - HARDWARE ACCESSORIES 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

Skinuvita Connector by Skinuvita GmbH — 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

Manufacturer
Skinuvita GmbH
EUDAMED SRN
DE-MF-000038977

Sources (1)

  • EUDAMED 17ecff9f-7780-41ce-ad56-98885fbb2392 61 fields · synced Jul 23, 2026