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Blade insert dia 50 large endoCupcut

EUDAMED

Class I (EU MDR)

Ref 780940 endocon catalogue Model Arthroplasty revision system

by endocon GmbH

Identity

Trade Name
Blade insert dia 50 large endoCupcut EUDAMED
Device Name
Revisionsinstrumentensystem EUDAMED
Model / Reference
Arthroplasty revision system EUDAMED
780940 endocon catalogue EUDAMED

Identifiers

Primary DI / UDI-DI
42514018006764 EUDAMED
Basic UDI-DI
4251401801512Q3 EUDAMED
Direct Marketing DI
42514018006764 EUDAMED
EMDN Code
L090999 ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHER 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

Category: Bone cutting forceps, reusable

Blade insert dia 50 large endoCupcut by endocon GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Bone cutting forceps, reusable.

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 d138ff88-440a-4e77-83ce-0ab40d5c4ed3 61 fields · synced Jun 17, 2026