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AdvaCyn Hydrogel

by Oculus Technologies of México S.A. de C.V. EUDAMED

Active European Union

Ref P-E200T00

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07502273990765 Basic UDI-DIDate17 Dec 2021RegisteredStatusActive

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  • Withdrawn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

Device Name
AdvaCyn Hydrogel
Model / Reference
P-E200T00
Primary DI / UDI-DI
07502273990765
Basic UDI-DI
B-07502273990765
EMDN Code
M04040501 Hydrogel dressings, non-combined
Device Class
Class IIb
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
MX-MF-000013827
Authorised representative
Sonoma Pharmaceuticals Netherlands B.V NL-AR-000013244

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See all devices from Oculus Technologies of México S.A. de C.V. →

Properties

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