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Katarakt-OP-Set

by Sengewald Klinikprodukte GmbH 85 variants

Ref 66229438-09Model 66231430-03

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 Number4034393CPTOPH2A2R Basic UDI-DI 04034393796956UDI-DIDate12 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  • Withdrawn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
Katarakt-Set
Model / Reference
66231430-03, 66229438-09
Primary DI / UDI-DI
04034393796956
Basic UDI-DI
4034393CPTOPH2A2R
EMDN Code
Q020601 Phacoemulsification sets
Device Class
Class IIa
Medical Purpose
Sterile, disposable procedure pack, combination of devices for disease treatment or modification of the anatomy related to ophthalmology.

Manufacturer details

EUDAMED SRN
DE-PR-000020748

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Properties

  • Sterile