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Ceren

by Ceren Üreti̇m Plasti̇k Ürünleri̇ Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇ 6 variants

Ref 2030 2060Model 2030-2061

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number868122707OGAT000LC Basic UDI-DI 08681227070018UDI-DIDate25 May 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  • Withdrawn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
Steri̇l Olmayan Atomi̇zer Chamber (Orta)
Model / Reference
2030-2061, 2030 2060
Primary DI / UDI-DI
08681227070018
Basic UDI-DI
868122707OGAT000LC
Direct Marketing DI
08681227070018
EMDN Code
R03010302 Aerosol portable inhalers
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000022140

Other devices from Ceren Üreti̇m Plasti̇k Ürünleri̇ Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇

See all devices from Ceren Üreti̇m Plasti̇k Ürünleri̇ Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇ →

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