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Innomed

by Zhejiang Longterm Medical Technology Co., Ltd. EUDAMED

Active European Union

Ref 5088

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69263655200057Y Basic UDI-DIDate16 Nov 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  • Withdrawn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
Hydrocolloid blister plaster
Model / Reference
5088
Primary DI / UDI-DI
06926365582637
Basic UDI-DI
69263655200057Y
Direct Marketing DI
06926365582637
EMDN Code
M04040301 Hydrocolloid dressings, non-combined
Device Class
Class IIa
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
CN-MF-000001161
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Zhejiang Longterm Medical Technology Co., Ltd.

See all devices from Zhejiang Longterm Medical Technology Co., Ltd. →

Properties

  • Sterile

Other properties (12)

  • 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