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Instramed

EUDAMED

Class I (EU MDR)

Ref S42-9105

by Farla Medical Ltd

Identity

Trade Name
Instramed EUDAMED
Device Name
Vasectomy forceps blunt/blunt EUDAMED
Model / Reference
S42-9105 EUDAMED

Identifiers

Primary DI / UDI-DI
D-S42-9105RX EUDAMED
Basic UDI-DI
B-S42-9105RX EUDAMED
EMDN Code
V9012 NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

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

Instramed by Farla Medical Ltd — Class I — 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European Union No Longer Active

CE/MDD

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Manufacturer

Manufacturer
Farla Medical Ltd
EUDAMED SRN
GB-MF-000003751
Authorised Representative
Farla Medical BVBA Limited BE-AR-000003667

Sources (1)

  • EUDAMED 9503f3c7-4e87-48e6-a881-8d2c8bafd81d 61 fields · synced Jun 18, 2026