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05993022948168

by Medicontur Medical Engineering Ltd. EUDAMED

Active European Union

Ref 05993022948168Model 877PETY

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number2023-MDR/QS-046/B Date11 Sep 2026IssuedStatusActive expires 10 Nov 2028

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 2023-MDR/QS-046/B Supplemented

    Quality management system EU MDR

    Notified body
    3EC International a.s. 2265
    Issued
    11 Sep 2026
    Expires
    10 Nov 2028
    Reason
    Other
  • 2023-MDR/TD-046/B Supplemented

    Technical documentation EU MDR

    Notified body
    3EC International a.s. 2265
    Issued
    11 Sep 2026
    Expires
    10 Nov 2028
    Reason
    Other

Specification

EUDAMED

Model / Reference
877PETY, 05993022948168
Primary DI / UDI-DI
05993022948168
Basic UDI-DI
599302877PETYRQ
EMDN Code
P030102090301 IOLs, APHAKIC, MONOFOCAL, TORIC, HYDROPHOBIC ACRYLIC
Device Class
Class IIb
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
HU-MF-000024195

Other devices from Medicontur Medical Engineering Ltd.

See all devices from Medicontur Medical Engineering Ltd. →

Properties

  • Sterile
  • Implantable

Other properties (12)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Sutures: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No