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Hak

EUDAMED

Class I (EU MDR)

Ref 30.1080.000Model Retractor

by ChM spółka z ograniczoną odpowiedzialnością

Identity

Device Name
Hak EUDAMED
Model / Reference
Retractor EUDAMED
30.1080.000 EUDAMED

Identifiers

Primary DI / UDI-DI
05908447023581 EUDAMED
Basic UDI-DI
59084472NL111M5 EUDAMED
EMDN Code
L03140199 SPREADERS AND RETRACTORS FOR GENERAL SURGERY, REUSABLE - OTHER 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: Hand-held surgical retractor, reusable

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

Similar devices

Also classified as Hand-held surgical retractor, reusable.

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 1b19bb8c-a302-4bdf-a2f2-449f7dd8a453 61 fields · synced Jun 18, 2026