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Hemi Arthroplasty Pack - SEHSCT

EUDAMED

Class I (EU MDR)

Ref 5060G

by Clonallon Laboratories Ltd

Identity

Trade Name
Hemi Arthroplasty Pack - SEHSCT EUDAMED
Device Name
Sterile Procedure Pack EUDAMED
Model / Reference
5060G EUDAMED

Identifiers

Primary DI / UDI-DI
05056745803982 EUDAMED
Basic UDI-DI
5060534890008VK EUDAMED
EMDN Code
V9012 NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE 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

Hemi Arthroplasty Pack - SEHSCT 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 (1)

  • EUDAMED 394a6fd4-48a6-4f16-961d-4f3b991af6cb 61 fields · synced Jul 22, 2026