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Citoplast Aqua

by Sopharma AD Bulgaria EUDAMED

Ref 32003000-0028, 32003000-0029 EMDN M04010102

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3800010632003293 Basic UDI-DIDate8 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  • Withdrawn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 · synced 22 Oct 2026

Device Name
Citoplast
Model / Reference
32003000-0028, 32003000-0029
Primary DI / UDI-DI
03800728497307, 03800728497314
Basic UDI-DI
3800010632003293
Direct Marketing DI
03800728497307
03800728497314
EMDN Code
M04010102 Polyurethane (or other material) adhesive dressings, with absorbent pad
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 & 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 (2)

  • EUDAMED 189dad1d-f1c7-4c30-a9ab-4cef05346cc3 61 fields · synced 22 Oct 2026
  • EUDAMED 03800728497314|3800010632003293 61 fields · synced 17 May 2026