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Osteotom Set

EUDAMED

Class I (EU MDR)

Ref 0020070 endocon catalogueModel Arthroplasty revision system

by endocon GmbH

Identity

Trade Name
Osteotom Set EUDAMED
Device Name
Revisionsinstrumentensystem EUDAMED
Model / Reference
Arthroplasty revision system EUDAMED
0020070 endocon catalogue EUDAMED

Identifiers

Primary DI / UDI-DI
42514018026700 EUDAMED
Basic UDI-DI
4251401801512Q3 EUDAMED
Direct Marketing DI
42514018026700 EUDAMED
EMDN Code
L090401 ORTHOPAEDIC SURGERY OSTEOTOMES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Osteotom Set by endocon GmbH — 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

Manufacturer
endocon GmbH
EUDAMED SRN
DE-MF-000020703

Sources (1)

  • EUDAMED 08d44dff-8150-4e99-b522-0f0b84ec7b7a 61 fields · synced Jun 19, 2026