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Aloclair Teething Gel

by Alliance Pharmaceuticals Limited EUDAMED

Active European Union

Model 5036631ALOCTGL800625

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5036631ALOCTGL800625 Basic UDI-DIDate8 Jul 2024RegisteredStatusActive

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  • Withdrawn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

Model / Reference
5036631ALOCTGL800625
Primary DI / UDI-DI
15036631009510
Basic UDI-DI
5036631ALOCTGL800625
EMDN Code
Q019007 Buccal topical treatment preparations not included in other classes
Device Class
Class IIa
Market of Registration
Northern 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

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