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Ophthalmic Reusable Pack

by Innolcon Medical Technology (Suzhou) Co., Ltd. EUDAMED

Active European Union

Ref FMSR300301Model FMSR100301, FMSR100302, FMSR100303, FMSR100304, FMSR200301, FMSR200302, FMSR200303, FMSR200304, FMSR300301, FMSR300302, FMSR300303、FMSR300304

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697246494MD03100ORPP001ZG Basic UDI-DIDate25 Oct 2024RegisteredStatusActive

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  • Withdrawn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

Model / Reference
FMSR100301, FMSR100302, FMSR100303, FMSR100304, FMSR200301, FMSR200302, FMSR200303, FMSR200304, FMSR300301, FMSR300302, FMSR300303、FMSR300304
Primary DI / UDI-DI
06972464944500
Basic UDI-DI
697246494MD03100ORPP001ZG
EMDN Code
Q020680 Phacoemulsification devices - accessories
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000012689
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Other devices from Innolcon Medical Technology (Suzhou) Co., Ltd.

See all devices from Innolcon Medical Technology (Suzhou) Co., Ltd. →

Properties

  • Sterile
  • Reusable
  • CMR Substance

Other properties (10)

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