International safety notice

• Unidad de tratamiento Intego • Unidad de tratamiento Intego Pro Unidades de tratamiento Intego/Intego Pro sin función Ergomotion.

Spain / AEMPS · ESP · May 6, 2021

Key facts

Title • Unidad de tratamiento Intego • Unidad de tratamiento Intego Pro Unidades de tratamiento Intego/Intego Pro sin función Ergomotion.
Regulator Spain / AEMPS
Country ESP
Brand • Unidad de tratamiento Intego • Unidad de tratamiento Intego Pro Unidades de tratamiento Intego/Intego Pro sin función Ergomotion.
Manufacturer Sirona Dental Systems GmbH, Alemania.
Models 28038, 16-2591, 91.822.52.89, DE49136990, 01-02-2021, 8254893, HYVEDEMM430, 67021, 582711800, 2021-252, 28022, DE191529171 and 2 more
Event type Safety Notice
Date May 6, 2021

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 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