International safety notice

Spiggle & Theis Medizintechnik

United Kingdom / MHRA · GBR · Nov 14, 2016

Key facts

Title Spiggle & Theis Medizintechnik
Regulator United Kingdom / MHRA
Country GBR
Brand Inflation device
Manufacturer Spiggle & Theis Medizintechnik
Models 2080-9030020
Event type Safety Notice
Action type Field safety notice
Date Nov 14, 2016
Regulator page gov.uk

At a glance

  • No Recall
  • Yes 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