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Vitalis

EUDAMED

Class I (EU MDR)

Ref SP0116

by PS Product Services GmbH

Identity

Trade Name
Vitalis EUDAMED
Device Name
Neopren-Bandagen EUDAMED
Model / Reference
SP0116 EUDAMED

Identifiers

Primary DI / UDI-DI
04050235001118 EUDAMED
Basic UDI-DI
4050235PS0005BJ EUDAMED
Direct Marketing DI
04050235001118 EUDAMED
EMDN Code
M0399 BANDAGES - OTHER (see Y06 for collars, tutors, etc.) 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 325b1048-7291-4162-83a6-237fabdf142f 61 fields · synced Jun 19, 2026