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RUDANAHT® 6 x 75 MM P3

EUDAMED

Class I (EU MDR)

Ref 060806

by NOBAMED Paul Danz AG

Identity

Trade Name
RUDANAHT® 6 x 75 MM P3 EUDAMED
Device Name
RUDANAHT® EUDAMED
Model / Reference
060806 EUDAMED

Identifiers

Primary DI / UDI-DI
04031815060824 EUDAMED
Basic UDI-DI
40318150600032 EUDAMED
EMDN Code
H900102 BANDAGES FOR SUTURES 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

RUDANAHT® 6 x 75 MM P3 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 bdb13859-3222-4d19-a776-772a811302d9 61 fields · synced Oct 6, 2026