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0.25 mL Fluoride/Oxalate Micro Blood Collection Tube, Grey Cap 10x45mm

by Ttt Sağlik Hi̇zmetleri̇ Eği̇ti̇m İnşaat Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

Ref 02508Model 2508

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-08682578825081 Basic UDI-DI 08682578825081UDI-DIDate8 Oct 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  • Withdrawn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/IVDD Active

Specification

EUDAMED

Model / Reference
2508, 02508
Primary DI / UDI-DI
08682578825081
Basic UDI-DI
B-08682578825081
EMDN Code
W0501010203 Blood collection, capillary tubes
Device Class
Class IVD General
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000045279

Other devices from Ttt Sağlik Hi̇zmetleri̇ Eği̇ti̇m İnşaat Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

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Properties

  • Professional Testing

Other properties (10)

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