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Zange, Tonsillen / Forceps, tonsils

EUDAMED

Class I (EU MDR)

Ref 51185-19

by REDA Instrumente GmbH

Identity

Device Name
Zange, Tonsillen / Forceps, tonsils EUDAMED
Model / Reference
51185-19 EUDAMED

Identifiers

Primary DI / UDI-DI
04063058046761 EUDAMED
Basic UDI-DI
4063058000001784D EUDAMED
Direct Marketing DI
04063058046761 EUDAMED
EMDN Code
L14010201 TONSILLARY PLIERS, 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

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

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 ba50c353-bec8-41de-836f-c6c6e0abdf17 61 fields · synced Aug 4, 2026