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Cybertech

by CB Healthcare Consulting GmbH 314 variants

Ref 5720397Model TF-152

Cybertech (5720397) is a Class IIa device made by CB Healthcare Consulting GmbH, registered in EUDAMED on 28 May 2026 (Basic UDI-DI B-14062183004162), active as of 23 Oct 2026.

Active European Union

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-14062183004162 Basic UDI-DI 14062183004162UDI-DIDate28 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Diamond Burs
Model / reference
TF-152, 5720397
Primary DI / UDI-DI
14062183004162
Basic UDI-DI
B-14062183004162
EMDN code
Q010501 Dental burs and abrasive disks, single-use
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005902

Other devices from CB Healthcare Consulting GmbH

See all devices from CB Healthcare Consulting GmbH →

Properties

  • Sterilise before use
Other properties (13, all answered No)