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MULLKOMPRESSEN 10x20 16FACH

EUDAMED

Class I (EU MDR)

Ref 857120

by NOBAMED Paul Danz AG

Identity

Trade Name
MULLKOMPRESSEN 10x20 16FACH EUDAMED
Device Name
MULLKOMPRESSEN EUDAMED
Model / Reference
857120 EUDAMED

Identifiers

Primary DI / UDI-DI
04031815816728 EUDAMED
Basic UDI-DI
4031815826005U EUDAMED
EMDN Code
M0201020102 COTTON GAUZES, FOLDED, WITHOUT X-RAY DETECTABLE THREAD, NON-STERILE 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

MULLKOMPRESSEN 10x20 16FACH 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 9a8e6a33-894c-4f70-ae33-304eb036f5bb 61 fields · synced Jun 20, 2026