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Canneff

by CB21 Pharma, s.r.o. Czech Republic EUDAMED

Ref CANNEFF SUP – rectal suppositoriesModel CANNEFF SUP – rectal suppositories REF 003, REF 005, REF 010 EMDN G05

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-859419703041SUP6F Basic UDI-DIDate5 May 2026RegisteredStatusActive

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  • Withdrawn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 24 Oct 2026

Device Name
CANNEFF SUP- rectal suppositories
Model / Reference
CANNEFF SUP – rectal suppositories REF 003, REF 005, REF 010, CANNEFF SUP – rectal suppositories
Primary DI / UDI-DI
859419703041SUP6F
Basic UDI-DI
B-859419703041SUP6F
EMDN Code
G05 Topical anorectal administered gastro-intestinal system devices
Device Class
Class IIb
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000037413

Other devices from CB21 Pharma, s.r.o.

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 3a13c6e3-793f-4ff1-9f89-837cbf51f607 61 fields · synced 24 Oct 2026