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Dental Endo Motor

by Chengdu Sani Medical Equipment Co., Ltd. 100 variants

Ref /Model FG—4

Active European Union

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06974242192202 Basic UDI-DI 06974242192202UDI-DIDate12 Jul 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Carbide Bur
Model / Reference
FG—4, /
Primary DI / UDI-DI
06974242192202
Basic UDI-DI
B-06974242192202
EMDN Code
L159007 Odontostomatology burs, reusable
Device Class
Class IIa
EU market of registration
Croatia

Manufacturer details

EUDAMED SRN
CN-MF-000011715
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Chengdu Sani Medical Equipment Co., Ltd

See all devices from Chengdu Sani Medical Equipment Co., Ltd →

Properties

  • Sterile
  • Reusable
  • Reprocessed

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No