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PROLENS de nuit

by Laboratoire Precilens EUDAMED

Active European Union

Ref PROLENS de nuit

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3666486OrthokpresbytieGT Basic UDI-DIDate3 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Drl
Many
Model / Reference
PROLENS de nuit
Primary DI / UDI-DI
03666486000803, 03666486000872, 03666486000834
Basic UDI-DI
3666486OrthokpresbytieGT, 3666486OrthoKmyopieUQ, 3666486Orthokametropie66
EMDN Code
Q02100499 Contact lenses - other
Device Class
Class IIa
Special Device Type
Made to order Rigid Gas Permeable (RGP) contact lenses
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000913

Other devices from Laboratoire Precilens

See all devices from Laboratoire Precilens →

Properties

Show properties
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: 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