International safety notice

Ανάκληση παρτίδων της ενδομήτριας συσκευής Nova T Για να δείτε την απόφαση, πατήστε εδώ

Greece / EOF · GRC · Jan 26, 2016

Key facts

Title Ανάκληση παρτίδων της ενδομήτριας συσκευής Nova T Για να δείτε την απόφαση, πατήστε εδώ
Regulator Greece / EOF
Country GRC
Manufacturer Bayer Ελλάς ΑΒΕΕ
Models TU011D8, TU013RL, 2040435, 18-20, 30.04.2017, TU00VBF, 18-12-2015, 90045, 130648, 6549500, 28.02.2018, 31.05.2018 and 1 more
Event type Recall, Safety Notice
Date Jan 26, 2016
Regulator page eof.gr

At a glance

  • Yes Recall
  • Yes Field safety notice
  • 1–9 Matching device models in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices