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Zange, Tupfer / Forceps, swabs

EUDAMED

Class I (EU MDR)

Ref 17233-26

by REDA Instrumente GmbH

Identity

Device Name
Zange, Tupfer / Forceps, swabs EUDAMED
Model / Reference
17233-26 EUDAMED

Identifiers

Primary DI / UDI-DI
04063058012346 EUDAMED
Basic UDI-DI
40630580000018244 EUDAMED
Direct Marketing DI
04063058012346 EUDAMED
EMDN Code
L031302 MEDICATION FORCEPS, REUSABLE 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: Dressing/utility forceps, tweezers-like, reusable

Zange, Tupfer / Forceps, swabs by REDA Instrumente GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dressing/utility forceps, tweezers-like, 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 44d7ee19-57e9-4332-9528-772df9cc16a1 61 fields · synced Sep 17, 2026