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Oído

EUDAMED

Class III (EU MDR)

Ref 2307441Model 3152

by Paul Hartmann Ag

Identity

Trade Name
Oído EUDAMED
Device Name
CombiSet ENTsurgery EUDAMED
Model / Reference
3152 EUDAMED
2307441 EUDAMED

Identifiers

Primary DI / UDI-DI
04099467198531 EUDAMED
Basic UDI-DI
40495003152KD 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

Oído 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 eb53068a-c548-4371-ab2f-acd53901033f 61 fields · synced Jul 15, 2026