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Vitalis

EUDAMED

Class I (EU MDR)

Ref FP0022

by PS Product Services GmbH

Identity

Trade Name
Vitalis EUDAMED
Device Name
Fußbandagen mit Geleinlage EUDAMED
Model / Reference
FP0022 EUDAMED

Identifiers

Primary DI / UDI-DI
04050235001804 EUDAMED
Basic UDI-DI
4050235PS0006BL EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

Category: Device sterilization/disinfection container, reusable

Vitalis by PS Product Services GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

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 ffb9275d-5744-428f-a8cd-bbf1fb957c61 61 fields · synced Jun 18, 2026