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Granusept

by CF Pharma Ireland Ltd Ireland EUDAMED

Ref FP1651Model Granusept MD 250ml Liquid Polish language EMDN V9099

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05907377532439 Basic UDI-DIDate5 Apr 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  • Withdrawn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 · synced 23 Oct 2026

Model / Reference
Granusept MD 250ml Liquid Polish language, FP1651
Primary DI / UDI-DI
05907377532439
Basic UDI-DI
B-05907377532439
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class IIa
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
IE-MF-000004595

Related devices

Category: Device sterilization/disinfection container, reusable

Other devices from CF Pharma Ireland Ltd

See all devices from CF Pharma Ireland Ltd →

Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • Implantable: No
  • 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

Sources (1)

  • EUDAMED 988286a4-bfd2-4c3b-b62f-d1409f0a063e 61 fields · synced 23 Oct 2026