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T5 Master

by Vitali S.R.L.

Part of a family of 11 devices: see the family page

Ref T5 MASTER

T5 Master is a Class IIa device made by Vitali S.R.L., registered in EUDAMED on 18 Jan 2023 (Basic UDI-DI B-08056201740124), active as of 24 Oct 2026.

Active European Union

CE MDR CE MDD

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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberB-08056201740124 Basic UDI-DI 08056201740124UDI-DIDate18 Jan 2023RegisteredStatusActive
European UnionCE/MDD NumberB-08056201740124 Basic UDI-DI 08056201740124UDI-DIDate18 Jan 2023RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR, CE/MDD Active

Specification

EUDAMED

Device name
Dental Unit
Model / reference
T5 MASTER
Primary DI / UDI-DI
08056201740124
Basic UDI-DI
B-08056201740124, 805620174991BM
Direct marketing DI
08056201740124
EMDN code
Z12110101 Dental treatment units
Device class
Class IIa
EU registration type
Legacy device (under a directive)
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000026752

Similar devices in this category

Other devices filed under DENTAL TREATMENT UNITS.

Other devices from Vitali S.R.L.

See all devices from Vitali S.R.L. →

Properties

  • Contains latex YesEUDAMEDNoEUDAMED
Other properties (13, all answered No)