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Retraktor

EUDAMED

Class I (EU MDR)

Ref 40.8872.050Model Retractor

by ChM spółka z ograniczoną odpowiedzialnością

Identity

Device Name
Retraktor EUDAMED
Model / Reference
Retractor EUDAMED
40.8872.050 EUDAMED

Identifiers

Primary DI / UDI-DI
05908447711969 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

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Manufacturer

EUDAMED SRN
PL-MF-000002121

Sources (1)

  • EUDAMED 72d78f31-42df-4cbc-979c-992e5214c429 61 fields · synced Jun 17, 2026