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Vacusera

by Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.Ş. 255 variants

Ref 236800W

Active European Union

CE IVDR

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number++M712235URINETUBEX3 Basic UDI-DI +M712236800W1$UDI-DIDate5 Aug 2026RegisteredStatusActive

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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Device Name
VACUSERA® Urine Tubes
Model / Reference
236800W
Primary DI / UDI-DI
+M712236800W1$
Basic UDI-DI
++M712235URINETUBEX3
Direct Marketing DI
+M712236800W1$
EMDN Code
W05010202 Urine collection, tubes
Device Class
Class A
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000025066

Other devices from Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.Ş.

See all devices from Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.Ş. →

Properties

  • Sterile

Other properties (10)

  • 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
  • New Device: No