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Kürette / Curette

EUDAMED

Class I (EU MDR)

Ref 71720-09

by REDA Instrumente GmbH

Identity

Device Name
Kürette / Curette EUDAMED
Model / Reference
71720-09 EUDAMED

Identifiers

Primary DI / UDI-DI
04063058058221 EUDAMED
Basic UDI-DI
4063058000000243H EUDAMED
Direct Marketing DI
04063058058221 EUDAMED
EMDN Code
L0901 ORTHOPAEDIC SURGERY SPOONS AND CURETTES, 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: Bone curette, reusable

Kürette / Curette by REDA Instrumente GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Bone curette, 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 89f74074-86ec-49d1-855f-f6da67e80fe5 61 fields · synced Sep 18, 2026