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Dehp

by CB Healthcare Consulting GmbH 816 variants

Ref 9794048Model TF-013

Dehp (9794048) is a Class IIa device made by CB Healthcare Consulting GmbH, registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI B-04062183055853), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04062183055853 Basic UDI-DI 04062183055853UDI-DIDate26 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Reamers
Model / reference
TF-013, 9794048
Primary DI / UDI-DI
04062183055853
Basic UDI-DI
B-04062183055853
EMDN code
Q010399 Surgical dental devices - other
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)