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K50F Continental

by CEFLA s.c.

Part of a family of 119 devices: see the family page

Ref 71MJ0000Model Dental Units

K50F Continental (71MJ0000) is a Class IIa device made by CEFLA s.c., registered in EUDAMED on 14 Oct 2025 (Basic UDI-DI 803383793TRDENTUNA001QY), active as of 24 Oct 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803383793TRDENTUNA001QY Basic UDI-DI 08033837936244UDI-DIDate14 Oct 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Dental Units, 71MJ0000
Primary DI / UDI-DI
08033837936244
Basic UDI-DI
803383793TRDENTUNA001QY
Direct marketing DI
08033837936244
EMDN code
Z12110101 Dental treatment units
Device class
Class IIa
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000009228

Similar devices in this category

Other devices filed under DENTAL TREATMENT UNITS.

Other devices from CEFLA s.c.

See all devices from CEFLA s.c. →

Properties

Other properties (14, all answered No)