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Etki̇n Tibbi̇ Ci̇hazlar

by Etki̇n Tibbi̇ Ci̇hazlar Sanayi̇ Ve Ti̇caret A.Ş. 6 variants

Ref ETC LED ANKA+ 101-MZ

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8683517921403C2 Basic UDI-DI 08683517921246UDI-DIDate9 Jun 2026RegisteredStatusActive

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  • Withdrawn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
Etc LED Anka+ 101-Mz Mobile LED Minor Surgery Light
Model / Reference
ETC LED ANKA+ 101-MZ
Primary DI / UDI-DI
08683517921246
Basic UDI-DI
8683517921403C2
EMDN Code
Z12010702 Mobile scialytic lamps
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
TR-MF-000016189

Other devices from Etki̇n Tibbi̇ Ci̇hazlar 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