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RUDAVEN®-universal

EUDAMED

Class I (EU MDR)

Ref 072386

by NOBAMED Paul Danz AG

Identity

Trade Name
RUDAVEN®-universal EUDAMED
Device Name
RUDAVEN® EUDAMED
Model / Reference
072386 EUDAMED

Identifiers

Primary DI / UDI-DI
04031815069421 EUDAMED
Basic UDI-DI
40318150662046 EUDAMED
EMDN Code
M04010202 POLYURETHANE FIXING DRESSINGS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

RUDAVEN®-universal by NOBAMED Paul Danz AG — 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-000000023

Sources (1)

  • EUDAMED 7fd65542-5940-4b8f-b7e1-bbd888436553 61 fields · synced Oct 6, 2026