Skip to content

opus stoma care liftplus medical adhesive remover non sting spray

by Alliance Pharmaceuticals Limited

Ref 5503Model 5036631LIFTPLSSP8027Q8

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5036631LIFTPLSSP8027Q8 Basic UDI-DI 15036631009916UDI-DIDate18 Jul 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Lift Plus Spray
Model / Reference
5036631LIFTPLSSP8027Q8, 5503
Primary DI / UDI-DI
15036631009916
Basic UDI-DI
5036631LIFTPLSSP8027Q8
EMDN Code
A108005 Devices for the removal of adhesives from the peristomal skin
Device Class
Class I
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000023165
Authorised representative
Alliance Pharma (Ireland) Ltd IE-AR-000022483

Other devices from Alliance Pharmaceuticals Limited

See all devices from Alliance Pharmaceuticals Limited →

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