International safety notice

Medtronic MiniMed 600 series insulin pumps - katkise või puduuva kinnitusrõngaga seadme kasutamisel insuliini üle- või alaannustamise oht

Estonia / EMDDB · EST · Nov 1, 2019

Key facts

Title Medtronic MiniMed 600 series insulin pumps - katkise või puduuva kinnitusrõngaga seadme kasutamisel insuliini üle- või alaannustamise oht
Regulator Estonia / EMDDB
Country EST
Brand Medtronic MiniMed 600 series insulin pumps
Manufacturer MEDTRONIC MINIMED 600 SERIES INSULIN PUMPS
Models MMT-1781, MMT-1782, MMT-1711, FA896, MMT-1780, MMT-1712
Date Nov 1, 2019
Regulator page terviseamet.ee

At a glance

  • No Recall
  • No Field safety notice

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