International safety notice

DT MedTech, LLC Hintermann Series H3 Total Ankle System - oodatust suurem seadme rikke oht

Estonia / EMDDB · EST · Jun 1, 2024

Key facts

Title DT MedTech, LLC Hintermann Series H3 Total Ankle System - oodatust suurem seadme rikke oht
Regulator Estonia / EMDDB
Country EST
Brand DT MedTech, LLC Hintermann Series H3 Total Ankle System
Manufacturer DT MEDTECH LLC HINTERMANN SERIES H3 TOTAL ANKLE SYSTEM
Models Tennessee37110, 302113, B095300607, B095302111, 300305, 302121, B095300505, B095301114, 300307, B095300507, B095300506, B095301123 and 110 more
Date Jun 1, 2024
Regulator page terviseamet.ee

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models in FDA data
  • 10–99 Matching catalog numbers 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