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RUDAVEN®-inject

EUDAMED

Class I (EU MDR)

Ref 072486

by NOBAMED Paul Danz AG

Identity

Trade Name
RUDAVEN®-inject EUDAMED
Device Name
RUDAVEN® EUDAMED
Model / Reference
072486 EUDAMED

Identifiers

Primary DI / UDI-DI
04031815069520 EUDAMED
Basic UDI-DI
40318150662046 EUDAMED
EMDN Code
M04010201 NON-WOVEN 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®-inject 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 d17024e5-5311-48d3-8308-50fc30b7967c 61 fields · synced Jun 19, 2026