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NOVAFIX SUPRA3 20g

by Laboratorios URGO S.L. EUDAMED

Withdrawn Not intended for the EU market

Ref ES0005299Model FÓRMULA ULTRAFUERTE

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8413647ULTRAFUERTEL8 Basic UDI-DIDate17 Jun 2022RegisteredStatusWithdrawn 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  • Withdrawn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European Union — CE/MDR Withdrawn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

0 certificates · EUDAMED

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

Specification

EUDAMED

Model / Reference
FÓRMULA ULTRAFUERTE, ES0005299
Primary DI / UDI-DI
08413647052998
Basic UDI-DI
8413647ULTRAFUERTEL8
Direct Marketing DI
08413647052998
EMDN Code
P01020180 Dental implants - accessories
Device Class
Class I

Manufacturer details

EUDAMED SRN
ES-MF-000000629

Other devices from Laboratorios URGO S.L.

See all devices from Laboratorios URGO S.L. →

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