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Vite

by IDI EVOLUTION S.r.l. 38 variants

Ref 700500Model VIT

Vite (700500) is a Class IIb device made by IDI EVOLUTION S.r.l., registered in EUDAMED on 16 Sep 2026 (Basic UDI-DI 805257021VITKD), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805257021VITKD Basic UDI-DI 08052570212880UDI-DIDate16 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Vite
Model / reference
VIT, 700500
Primary DI / UDI-DI
08052570212880
Basic UDI-DI
805257021VITKD
EMDN code
P01020180 Dental implants - accessories
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000005920

Similar devices in this category

Other devices filed under DENTAL IMPLANTS - ACCESSORIES.

Other devices from IDI EVOLUTION S.r.l.

See all devices from IDI EVOLUTION S.r.l. →

Properties

  • Sterilise before use
  • Implantable
  • Sutures
Other properties (12, all answered No)