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FUE Transplant Instrument Set

EUDAMED

Class I (EU MDR)

Ref 5001CRef 5001

by Clonallon Laboratories Ltd

Identity

Trade Name
FUE Transplant Instrument Set EUDAMED
Device Name
Sterile Procedure Pack EUDAMED
Model / Reference
5001C EUDAMED
5001 EUDAMED

Identifiers

Primary DI / UDI-DI
05056745804415 EUDAMED
05056745804057 EUDAMED
Basic UDI-DI
5060534890008VK EUDAMED
EMDN Code
V9012 NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE EUDAMED
V0599 CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Medical Purpose
Non-Specialist Surgical Instruments and Kits, Single-Use EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

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

FUE Transplant Instrument Set by Clonallon Laboratories Ltd — Class I — MDR — 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/MDR

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Manufacturer

EUDAMED SRN
XI-PR-000033753

Sources (2)

  • EUDAMED f47da037-7e48-4cde-ba4a-88ea2a21fd12 61 fields · synced Sep 18, 2026
  • EUDAMED 2f986ff4-cd75-46a1-b09c-35cc6d3eeb1e 61 fields · synced May 17, 2026