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TransFix and TransFix Sample Storage Tubes

by Caltag Medsystems Ltd EUDAMED

Active European Union

Ref TF-01-10

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number506053171TFBSST7P Basic UDI-DIDate29 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/IVDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
TransFix and TransFix Sample Storage Tubes
Model / Reference
TF-01-10
Primary DI / UDI-DI
25060531710037
Basic UDI-DI
506053171TFBSST7P
Direct Marketing DI
25060531710037
EMDN Code
W050301020101 Samples analyses, plastic tubes with additives
Device Class
Class A
Market of Registration
Austria

Manufacturer details

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

Other devices from Caltag Medsystems Ltd

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Properties

  • Reagent
  • Professional Testing

Other properties (9)

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