← Back to catalogue

Ring Curette-Teardrop

EUDAMED

Class I (EU MDR)

Ref 0402-431Model 0402-430

by Meditec Source GmbH & Co. KG

Identity

Device Name
Ring Curette-Teardrop EUDAMED
Model / Reference
0402-430 EUDAMED
0402-431 EUDAMED

Identifiers

Primary DI / UDI-DI
04262463852466 EUDAMED
Basic UDI-DI
426246385PG049M EUDAMED
Direct Marketing DI
04262463852466 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

Ring Curette-Teardrop by Meditec Source GmbH & Co. KG — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000006490

Sources (1)

  • EUDAMED 591dfe58-c73a-400d-bd5d-2fbc05abd33f 61 fields · synced Jul 31, 2026