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Nobadrape® Anästhesietuch 120x150 Cm Loch 10cm

EUDAMED

Class I (EU MDR)

Ref 800150

by NOBAMED Paul Danz AG

Identity

Trade Name
NOBADRAPE® ANÄSTHESIETUCH 120X150 CM LOCH 10CM EUDAMED
Device Name
NOBADRAPE® EUDAMED
Model / Reference
800150 EUDAMED

Identifiers

Primary DI / UDI-DI
04031815725556 EUDAMED
Basic UDI-DI
4031815711004H EUDAMED
EMDN Code
T020199 SURGICAL DRAPES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

Nobadrape® Anästhesietuch 120x150 Cm Loch 10cm 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 a3d3ba16-f751-4ec1-9faa-ed01cc8798fd 61 fields · synced Jul 19, 2026