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Curette

EUDAMED

Class IIa (EU MDR)

Ref 8001765Ref 8001750

by Applimed SA

Identity

Device Name
Curette EUDAMED
Model / Reference
8001765 EUDAMED
8001750 EUDAMED

Identifiers

Primary DI / UDI-DI
07640178432765 EUDAMED
07640178430181 EUDAMED
Basic UDI-DI
B-07640178432765 EUDAMED
B-07640178430181 EUDAMED
EMDN Code
V9012 NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Curette by Applimed SA — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Applimed SA
EUDAMED SRN
CH-MF-000046641
Authorised Representative
Dansu A/S DK-AR-000046254

Sources (2)

  • EUDAMED 02b995be-4c2f-4698-b23e-8e48797181ef 61 fields · synced Jul 14, 2026
  • EUDAMED b3eb8aca-7ae4-4fb6-89db-095674f4351c 61 fields · synced May 17, 2026