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Tussipect Adult

by Ste Pharmaceuticals, S.L.U Spain EUDAMED

Ref PL0235_140 EMDN Q030199

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number843661764PL0235BY Basic UDI-DIDate1 Jul 2026RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
Cough Syrup Hedera
Model / Reference
PL0235_140
Primary DI / UDI-DI
08436617649639
Basic UDI-DI
843661764PL0235BY
EMDN Code
Q030199 Nasopharyngeal devices - other
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
ES-MF-000000144

Other devices from Ste Pharmaceuticals, S.L.U

See all devices from Ste Pharmaceuticals, S.L.U →

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 (1)

  • EUDAMED 08436617649639|843661764PL0235BY 61 fields · synced 25 Oct 2026