EUDAMED last updated this device on Sep 22, 2023
TransFix 1ml
506053171TFBSST7POn the marketIVDR Class A
- Applicable legislation
- —
- Organization name
- Caltag Medsystems Ltd
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →- 05060531710026
- Reference / catalog number
- TFB-01-1, TFB-01-10, TFB-01-50
Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.
TransFix 1ml is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Caltag Medsystems Ltd. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.