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Súprava na Herniu NUDCH BA

EUDAMED

Class III (EU MDR)

Ref 2479687Model 3142

by Paul Hartmann Ag

Identity

Trade Name
Súprava na Herniu NUDCH BA EUDAMED
Device Name
CombiSet General surgery EUDAMED
Model / Reference
3142 EUDAMED
2479687 EUDAMED

Identifiers

Primary DI / UDI-DI
04099467181526 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

Category: Ophthalmic surgical procedure kit, non-medicated, single-use

Súprava na Herniu NUDCH BA by Paul Hartmann Ag — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical procedure kit, non-medicated, single-use.

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 e9c24c96-8536-4b05-b34a-b6b284981ddd 61 fields · synced Jul 16, 2026