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Rudaclude® S

EUDAMED

Class I (EU MDR)

Ref 050030

by NOBAMED Paul Danz AG

Identity

Trade Name
RUDACLUDE® S EUDAMED
Device Name
RUDACLUDE® EUDAMED
Model / Reference
050030 EUDAMED

Identifiers

Primary DI / UDI-DI
04031815050320 EUDAMED
Basic UDI-DI
40318150503034 EUDAMED
EMDN Code
M04010101 NON-WOVEN ADHESIVE DRESSINGS, WITH ABSORBENT PAD 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

Rudaclude® S 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 c3f29953-53be-4a73-904e-2e696a3f1a22 61 fields · synced Oct 6, 2026