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Sanplast Citofilm

by Sopharma AD EUDAMED

Active European Union

Ref 32003000-0016

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number380001063200318Z Basic UDI-DIDate11 Aug 2022RegisteredStatusActive

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  • Withdrawn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

Device Name
Sanplast
Model / Reference
32003000-0016
Primary DI / UDI-DI
03800728496881
Basic UDI-DI
380001063200318Z
Direct Marketing DI
03800728496881
EMDN Code
M050101 Plasters on spools (rolls)
Device Class
Class I
Market of Registration
Bulgaria

Manufacturer details

EUDAMED SRN
BG-MF-000019983

Other devices from Sopharma AD

See all devices from Sopharma AD →

Properties

Show properties
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