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Lap. Hernie

EUDAMED

Class III (EU MDR)

Ref 2306801Model 3142

by Paul Hartmann Ag

Identity

Trade Name
Lap. Hernie EUDAMED
Device Name
CombiSet General surgery EUDAMED
Model / Reference
3142 EUDAMED
2306801 EUDAMED

Identifiers

Primary DI / UDI-DI
04099467202634 EUDAMED
Basic UDI-DI
40495003142KA EUDAMED
EMDN Code
V0599 CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class III EUDAMED
Medical Purpose
A CombiSet is characterized by the customized compilation of defined components used for medical treatments. These are single-use products for surgical procedures. EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Lap. Hernie by Paul Hartmann Ag — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Paul Hartmann Ag
EUDAMED SRN
DE-PR-000019925

Sources (1)

  • EUDAMED c5855d32-3e43-4b1b-9000-176138c25ae4 61 fields · synced Jul 12, 2026