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Pince - Kocher Forceps

EUDAMED

Class IIa (EU MDR)

Ref 8001030

by Applimed SA

Identity

Device Name
Pince - Kocher Forceps EUDAMED
Model / Reference
8001030 EUDAMED

Identifiers

Primary DI / UDI-DI
07640178437760 EUDAMED
Basic UDI-DI
B-07640178437760 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

Category: Surgical retractor/retraction system blade, single-use

Pince - Kocher Forceps by Applimed SA — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, single-use.

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 (1)

  • EUDAMED ba3cfd5b-7a86-4b33-bc02-0d6a82bfe31c 61 fields · synced Aug 2, 2026