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Zollikerberg Procedure Pack 2025

EUDAMED

Class I (EU MDR)

Ref 6161E

by Clonallon Laboratories Ltd

Identity

Trade Name: Zollikerberg Procedure Pack 2025 EUDAMED
Device Name: Sterile Procedure Pack EUDAMED
Model / Reference: 6161E EUDAMED

Identifiers

Primary DI / UDI-DI: 05056745803302 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

Zollikerberg Procedure Pack 2025 by Clonallon Laboratories Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

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

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Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer: Clonallon Laboratories Ltd
EUDAMED SRN: XI-PR-000033753

Sources (1)

EUDAMED 0442a46a-5999-477f-ae14-5249a64ee519 61 fields · synced Jul 14, 2026