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Vitalis

EUDAMED

Class I (EU MDR)

Ref FP0018

by PS Product Services GmbH

Identity

Trade Name
Vitalis EUDAMED
Device Name
Fuß- und Finger-Druckschutz EUDAMED
Model / Reference
FP0018 EUDAMED

Identifiers

Primary DI / UDI-DI
04050235000609 EUDAMED
Basic UDI-DI
4050235PS0004BG EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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

Vitalis by PS Product Services 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

EUDAMED SRN
DE-MF-000005290

Sources (1)

  • EUDAMED aaac25a3-1739-4b27-a3bc-f8e563b8ac2a 61 fields · synced Jun 18, 2026