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Duografter Ii

by Fidia Farmaceutici S.p.A. Italy EUDAMED

Ref 10001006Model TP03-01-01

EMDN V9099

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number80336618005030100000000RP Basic UDI-DIDate4 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Model / Reference
TP03-01-01, 10001006
Primary DI / UDI-DI
08033661808915
Basic UDI-DI
80336618005030100000000RP
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class IIa
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
IT-MF-000026988

Other devices from Fidia Farmaceutici S.p.A.

See all devices from Fidia Farmaceutici S.p.A. →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 08033661808915|80336618005030100000000RP 61 fields · synced 25 Oct 2026