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Zange, Tupfer / Forceps, swabs

EUDAMED

Class I (EU MDR)

Ref 17229-25

by REDA Instrumente GmbH

Identity

Device Name
Zange, Tupfer / Forceps, swabs EUDAMED
Model / Reference
17229-25 EUDAMED

Identifiers

Primary DI / UDI-DI
04063058012315 EUDAMED
Basic UDI-DI
40630580000018244 EUDAMED
Direct Marketing DI
04063058012315 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 644676f3-e6b1-433a-a9b0-273351d108c1 61 fields · synced Aug 2, 2026