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Wundhaken / Retractors

EUDAMED

Class I (EU MDR)

Ref R020-000000-010

by REDA Instrumente GmbH

Identity

Device Name
Wundhaken / Retractors EUDAMED
Model / Reference
R020-000000-010 EUDAMED

Identifiers

Primary DI / UDI-DI
04063058195353 EUDAMED
Basic UDI-DI
4063058000000153G EUDAMED
Direct Marketing DI
04063058195353 EUDAMED
EMDN Code
L03140199 SPREADERS AND RETRACTORS FOR GENERAL SURGERY, 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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Hand-held surgical retractor, reusable

Wundhaken / Retractors by REDA Instrumente GmbH — 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
DE-MF-000005592

Sources (1)

  • EUDAMED 1889be38-9b2d-47fd-a09e-71da0f8c32ef 61 fields · synced Jun 18, 2026