International safety notice

Analizador EXENT® Número de catálogo: IE800 UDI: 05051700020879

Spain / AEMPS · ESP · Apr 16, 2024

Key facts

Title Analizador EXENT® Número de catálogo: IE800 UDI: 05051700020879
Regulator Spain / AEMPS
Country ESP
Brand Analizador EXENT® Número de catálogo: IE800 UDI: 05051700020879
Manufacturer The Binding Site Group limited. Reino Unido
Models 91.822.52.89, IE800, 2024-194, 1.0.14, 05051700020879, 28022, SOFTWARE1.0.12, 08038, 900320400, 2749–2753, AE067, 105000 and 6 more
Event type Safety Notice
Date Apr 16, 2024

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

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