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Hernia Procedure Pack

EUDAMED

Class III (EU MDR)

Ref BOX09613V1

by Covidien llc

Identity

Device Name
Hernia Procedure Pack EUDAMED
Model / Reference
BOX09613V1 EUDAMED

Identifiers

Primary DI / UDI-DI
00824846001744 EUDAMED
Basic UDI-DI
0763000B00009027X EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class III EUDAMED
Medical Purpose
Херния EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Category: Device sterilization/disinfection container, reusable

Hernia Procedure Pack by Covidien llc — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Covidien llc
EUDAMED SRN
US-PR-000013794

Sources (1)

  • EUDAMED 58ced624-caab-419a-bb0a-99f980ced080 61 fields · synced Jul 25, 2026