Skip to content

Cyber Force

by Üzümcü Hastane Eki̇pmanlari Metal İşleme Sanayi̇ Ve Ti̇caret A.Ş. 49 variants

Ref CL-6D

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

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/MDR Number868322909950011VT Basic UDI-DI 08683229041188UDI-DIDate18 Nov 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Class 1
Model / Reference
CL-6D
Primary DI / UDI-DI
08683229041188
Basic UDI-DI
868322909950011VT
Direct Marketing DI
08683229041188
EMDN Code
Z12010702 Mobile scialytic lamps
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000018941

Other devices from Üzümcü Hastane Eki̇pmanlari Metal İşleme Sanayi̇ Ve Ti̇caret A.Ş.

See all devices from Üzümcü Hastane Eki̇pmanlari Metal İşleme Sanayi̇ Ve Ti̇caret A.Ş. →

Properties

Other properties (13)

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