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Ayset

by Ayset Tibbi Urunler Ve Plastik Tekstil Elektronik Gida Temizlik Maddeleri Insaat Muteahhitlik Sanayi A.S. 32 variants

Ref 70650

Active European Union

CE IVDD

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-08697427701515 Basic UDI-DI 08697427701515UDI-DIDate27 May 2025RegisteredStatusActive

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  • Withdrawn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/IVDD Active

Specification

EUDAMED

Device Name
Single Use Urine Container
Model / Reference
70650
Primary DI / UDI-DI
08697427701515
Basic UDI-DI
B-08697427701515
EMDN Code
W05010203 Urine collection, containers
Device Class
Class IVD General
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000016409

Other devices from Ayset Tibbi Urunler Ve Plastik Tekstil Elektronik Gida Temizlik Maddeleri Insaat Muteahhitlik Sanayi A.S.

See all devices from Ayset Tibbi Urunler Ve Plastik Tekstil Elektronik Gida Temizlik Maddeleri Insaat Muteahhitlik Sanayi A.S. →

Properties

Other properties (10)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No