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Lasik-OP-Set

by Sengewald Klinikprodukte GmbH

Ref 66231589-03Model 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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4034393CPTOPH2A2R Basic UDI-DI 04034393814223UDI-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  • Withdrawn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, 66231589-03
Primary DI / UDI-DI
04034393814223
Basic UDI-DI
4034393CPTOPH2A2R
EMDN Code
A010599 Ophthalmology injection needles and kits - other
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