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Equipamento Odontológico Sprint Titanium

by Olsen Indústria e Comércio SA

Ref 990040054Model Equipamento Odontológico Sprint Titanium

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

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 Number90888SPRINTTITANIUMFP Basic UDI-DI 17898971838292UDI-DIDate21 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Equipamento Odontológico Sprint Titanium, 990040054
Primary DI / UDI-DI
17898971838292
Basic UDI-DI
90888SPRINTTITANIUMFP
EMDN Code
V08020199, Z12110101
Device Class
Class I
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
BR-MF-000029450
Authorised representative
Cinterqual-Soluções de Comércio Internacional,Lda. PT-AR-000002813

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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