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Katarakt Set

by Paul Hartmann AG 15 variants

Ref 2340732Model 3151

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40495003151KB Basic UDI-DI 04099467082878UDI-DIDate26 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
CombiSet Ophthalmology
Model / Reference
3151, 2340732
Primary DI / UDI-DI
04099467082878
Basic UDI-DI
40495003151KB
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class III
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.

Manufacturer details

EUDAMED SRN
DE-PR-000019925

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Properties

  • Sterile