Technidata S.A.

FDA Regulatory Profile

Technidata S.A. appears in FDA public data with 4 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1573-2023, Class II) was initiated on March 27, 2023.

Summary

Total Recalls
4
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1573-2023Class IITDHisto/Cyto - A software product used for managing medical information in the field of laboratoriesMarch 27, 2023
Z-1310-2014Class IIITDWorkstation version 11.01.A or higher. TDWorkstation Evolution. TDWorkstation receives patient February 17, 2014
Z-1743-2013Class IIITDHistology/Cytology Classification name: Calculator/data processing module for clinical use (862June 20, 2013
Z-1345-2013Class IITD-Synergy. Laboratory Information System.July 29, 2010