International safety notice
Philips IntelliVue MX700 / MX800 Patient Monitors
Ireland / HPRA · IRL · Aug 5, 2020
Key facts
| Title | Philips IntelliVue MX700 / MX800 Patient Monitors |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | Philips IntelliVue MX700 / MX800 Patient Monitors |
| Manufacturer | Philips Medical Systems |
| Models | DE50887321, DE50887025, DE50887164, DE50887064, DE50887137, DE50887196, DE58562415, FSN86201913, DE58562344, DE50887179, MX800, DE58562353 and 21 more |
| Event type | Safety Notice |
| Date | Aug 5, 2020 |
| Regulator page | hpra.ie |
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