Skip to content

Halibut Feridas (50 g)

by Medinfar Manufacturing S.A.

Ref 7112862Model HF71128

Active European Union

CE MDR

Valid until

28 Jul 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DQS Medizinprodukte GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number1000225294 Date29 Jul 2026IssuedStatusActive expires 28 Jul 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 1000225294 Active

    Quality management system EU MDR

    Certifier
    DQS Medizinprodukte GmbH 0297
    Issued
    29 Jul 2026
    Expires
    28 Jul 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Halibut Feridas
Model / Reference
HF71128, 7112862
Primary DI / UDI-DI
05600903501366
Basic UDI-DI
560090350HF71128PE
EMDN Code
M9002 Protective devices, lubricants and soothing devices (sprays, gels, fluids and creams)
Device Class
Class IIb
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000012404

Other devices from Medinfar Manufacturing S.A.

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