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Integral dental unit

by Foshan Chuangxin Medical Apparatus Co., Ltd 9 variants

Ref CX-8900

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06975582138905 Basic UDI-DI 06975582138905UDI-DIDate30 Jul 2022RegisteredStatusActive

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  • Withdrawn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

Model / Reference
CX-8900
Primary DI / UDI-DI
06975582138905
Basic UDI-DI
B-06975582138905
EMDN Code
Z12110101 Dental treatment units
Device Class
Class IIa
EU market of registration
Latvia

Manufacturer details

EUDAMED SRN
CN-MF-000011665
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Foshan Chuangxin Medical Apparatus Co., Ltd

See all devices from Foshan Chuangxin Medical Apparatus Co., Ltd →

Properties

Other properties (11)

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