← Back to catalogue

Retraktor

EUDAMED

Class I (EU MDR)

Ref 40.8763.040Model Retractor

by ChM spółka z ograniczoną odpowiedzialnością

Identity

Device Name
Retraktor EUDAMED
Model / Reference
Retractor EUDAMED
40.8763.040 EUDAMED

Identifiers

Primary DI / UDI-DI
05908447385207 EUDAMED
Basic UDI-DI
59084472NL050MA EUDAMED
EMDN Code
L091002 INSTRUMENTS FOR PROCESSING MATERIALS FOR OSTEOSYNTHESIS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Wire holding/twisting forceps

Retraktor by ChM spółka z ograniczoną odpowiedzialnością — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Wire holding/twisting forceps.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
PL-MF-000002121

Sources (1)

  • EUDAMED 3b35a0a3-81c3-4b3d-89d7-c699bf8ccd0f 61 fields · synced Jun 18, 2026