International safety notice

Código del producto Modelo de producto Versión de software Identificador de dispositivo 728333 Spectral CT 7500 5.0 (01)00884838101111(21) 728334 Spectral CT on Rails 5.1.0.X (01)00884838103627(21) 728340 Spectral CT 7500 China 5.0 No aplicable

Spain / AEMPS · ESP · Jan 22, 2024

Key facts

Title Código del producto Modelo de producto Versión de software Identificador de dispositivo 728333 Spectral CT 7500 5.0 (01)00884838101111(21) 728334 Spectral CT on Rails 5.1.0.X (01)00884838103627(21) 728340 Spectral CT 7500 China 5.0 No aplicable
Regulator Spain / AEMPS
Country ESP
Brand Código del producto Modelo de producto Versión de software Identificador de dispositivo 728333 Spectral CT 7500 5.0 (01)00884838101111(21) 728334 Spectral CT on Rails 5.1.0.X (01)00884838103627(21) 728340 Spectral CT 7500 China 5.0 No aplicable
Manufacturer Philips Medical Systems Nederland B.V., Holanda.
Models 2023-PD-CTAMI-017, 728334, 00884838101111, FCO72800808, 2024-032, 728340, 28050, 28022, 00884838103627, 5.1.0.X, 91.822.52.89, 101069 and 1 more
Event type Safety Notice
Date Jan 22, 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

Browse all International device safety notices