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Implante Sistema Duo 3.8 X 8.5mm

by Signo Vinces Equipamentos Odontológicos EIRELI

Ref 21.201Model 21.201 IMPLANTE SISTEMA DUO 3.8 X 8.5MM

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD NumberB-07908688106430 Basic UDI-DI 07908688106430UDI-DIDate17 Jun 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
21.201 Implante Sistema Duo 3.8 X 8.5mm
Model / Reference
21.201 IMPLANTE SISTEMA DUO 3.8 X 8.5MM, 21.201
Primary DI / UDI-DI
07908688106430
Basic UDI-DI
B-07908688106430
EMDN Code
P01020101 Dental implants
Device Class
Class IIb
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
BR-MF-000011862
Authorised representative
SIGNO VINCES EUROPA, LDA PT-AR-000010057

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Properties

  • Sterile
  • Implantable

Other properties (9)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No