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Golamir Comprimidos para disolver en la boca

by Aboca S.P.A. Società Agricola Italy EUDAMED

Ref 08032472029939

EMDN V9017

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberEPT 0477.MDR.24/5352.3 Date30 Jul 2026IssuedStatusActive expires 2 Nov 2028

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • EPT 0477.MDR.24/5352.3 Reissued

    Quality management system EU MDR

    Notified body
    Notified body 0477
    Issued
    30 Jul 2026
    Expires
    2 Nov 2028

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Golamir compresse da sciogliere in bocca
Model / Reference
08032472029939
Primary DI / UDI-DI
08032472029939
Basic UDI-DI
8032472GOL2ax1V8
EMDN Code
V9017 Oral administration preparations not included in other classes
Device Class
Class IIa
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
IT-MF-000029499

Other devices from Aboca S.P.A. Società Agricola

See all devices from Aboca S.P.A. Società Agricola →

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 7b18aeb8-a6fe-4334-b1a4-0ce6452815db 61 fields · synced 22 Oct 2026