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TREPHINE Bur for Machine

by Dentis Co., Ltd 6 variants

Ref DTREBM50

TREPHINE Bur for Machine (DTREBM50) is a Class IIa device made by Dentis Co., Ltd., registered in EUDAMED on 7 Oct 2026 (Basic UDI-DI B-08806169140401), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08806169140401 Basic UDI-DI 08806169140401UDI-DIDate7 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
DTREBM50
Primary DI / UDI-DI
08806169140401
Basic UDI-DI
B-08806169140401
EMDN code
P01020180 Dental implants - accessories
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
KR-MF-000012523
Authorised representative
BEST FIT IMPLANTS S.A. ES-AR-000048728

Other devices from Dentis Co., Ltd.

See all devices from Dentis Co., Ltd. →

Properties

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