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Kompozyt kościozastępczy FlexiOss®

by Medical Inventi S.A. EUDAMED

Active European Union

Ref FlexiOss-5

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05903728887029 Basic UDI-DIDate13 Mar 2023RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
FlexiOss
Model / Reference
FlexiOss-5
Primary DI / UDI-DI
05903728887029, 05903728887050
Basic UDI-DI
B-05903728887029, B-05903728887050
EMDN Code
P900403 Non-resorbable filling and reconstruction devices
Device Class
Class IIb
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000007157

Other devices from Medical Inventi S.A.

Properties

Show properties
  • Sterile
  • Implantable
Other properties (9)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No