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Medosel Medi̇kal Anoni̇m Şi̇rketi̇

by Medosel Medi̇kal A.Ş. 2 variants

Ref 10308Model Lucca 10.190A

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-08682276275355 Basic UDI-DI 08682276275355UDI-DIDate14 Dec 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  • Withdrawn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

Device Name
Muayene Uniti,Endoskopi Taşıma Kollu,Uv sterilizatorlü(ENT Unit, Uv sterilizer)
Model / Reference
Lucca 10.190A, 10308
Primary DI / UDI-DI
08682276275355
Basic UDI-DI
B-08682276275355
EMDN Code
Z121402 ENT treatment units
Device Class
Class IIa
Special Device Type
-1192
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000014935

Related devices

Category: ENT examination/treatment system

Other devices from Medosel Medi̇kal A.Ş.

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