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Arthrosamid®

EUDAMED

Class IIb (EU MDR)

Ref 50020

by Contura International A/S

Identity

Trade Name
Arthrosamid® EUDAMED
Device Name
Arthrosamid® EUDAMED
Model / Reference
50020 EUDAMED

Identifiers

Primary DI / UDI-DI
05704101500203 EUDAMED
Basic UDI-DI
5704101Arthrosamid3K EUDAMED
EMDN Code
P900403 NON-RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Denmark EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

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

Arthrosamid® by Contura International A/S — Class IIb — 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
DK-MF-000002018

Sources (1)

  • EUDAMED 0b898010-6da0-4be1-a7d0-f33ac6a099e4 61 fields · synced Jun 17, 2026