International safety notice
Equipos de resonancia magnética de 1.5 T: Achieva 1.5T, Achieva 1.5T Conversion, Ingenia 1.5T CX, Intera 1.5T, Intera 1.5T Power/Pulsar y SmartPath a dStream para sistemas de 1.5 T.
Spain / AEMPS · ESP · Nov 14, 2023
Key facts
| Title | Equipos de resonancia magnética de 1.5 T: Achieva 1.5T, Achieva 1.5T Conversion, Ingenia 1.5T CX, Intera 1.5T, Intera 1.5T Power/Pulsar y SmartPath a dStream para sistemas de 1.5 T. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Equipos de resonancia magnética de 1.5 T: Achieva 1.5T, Achieva 1.5T Conversion, Ingenia 1.5T CX, Intera 1.5T, Intera 1.5T Power/Pulsar y SmartPath a dStream para sistemas de 1.5 T. |
| Manufacturer | Philips Healthcare, Países Bajos. |
| Models | 30004, 33534, 33408, 781260, 22330, 72048, 39095, 39003, 33692, 30297, 77067, 18038 and 805 more |
| Event type | Safety Notice |
| Date | Nov 14, 2023 |
At a glance
- No Recall
- Yes Field safety notice
- 1,000+ Matching device models in FDA data
- 1,000+ 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