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TransFix/EDTA 9 mL Vacuum Blood Collection Tubes (1 Tube)

by Caltag Medsystems Ltd

Ref TVT-09-1

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-35060531711611 Basic UDI-DI 35060531711611UDI-DIDate26 May 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  • Withdrawn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/IVDD Active

Specification

EUDAMED

Device Name
TransFix/EDTA 9 mL Vacuum Blood Collection Tubes (1 Tube)
Model / Reference
TVT-09-1
Primary DI / UDI-DI
35060531711611
Basic UDI-DI
B-35060531711611
EMDN Code
W050101010201 Blood collection, tubes with additives or serum separator
Device Class
Class IVD General
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
GB-MF-000021669
Authorised representative
Advena Limited MT-AR-000000234

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Properties

  • Sterile
  • Professional Testing

Other properties (8)

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