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Rudadetec®-Fingerkuppenpflaster

EUDAMED

Class I (EU MDR)

Ref 040100

by NOBAMED Paul Danz AG

Identity

Trade Name
RUDADETEC®-FINGERKUPPENPFLASTER EUDAMED
Device Name
RUDADETEC® EUDAMED
Model / Reference
040100 EUDAMED

Identifiers

Primary DI / UDI-DI
04031815040321 EUDAMED
Basic UDI-DI
4031815040302V EUDAMED
EMDN Code
M04010102 POLYURETHANE (OR OTHER MATERIAL) 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

Rudadetec®-Fingerkuppenpflaster 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 cd44cb03-a5e4-45d9-b8ea-cf86e9edbc5e 61 fields · synced Oct 6, 2026