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Bandomieji rėmeliai

by UAB Kavita EUDAMED

Active European Union

Ref KID/56, KID/52, RB-301/1Model KID

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4772208KIDEK Basic UDI-DIDate12 Mar 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Trial frame
Model / Reference
KID, KID/56, KID/52, RB-301/1
Primary DI / UDI-DI
04772208142764, 04772208142771, 04772208116468
Basic UDI-DI
4772208KIDEK, 4772208RB-301/16N
EMDN Code
Q0299 Ophthalmic devices - other
Device Class
Class I
Market of Registration
Lithuania

Manufacturer details

EUDAMED SRN
LT-MF-000002717

Other devices from UAB Kavita

See all devices from UAB Kavita →

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