International safety notice
Maquet - Getinge QUADROX-i Neonatal Microporous Membrane Oxygenator
United Kingdom / MHRA · GBR · May 10, 2019
Key facts
| Title | Maquet - Getinge QUADROX-i Neonatal Microporous Membrane Oxygenator |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Maquet - Getinge QUADROX-i Neonatal Microporous Membrane Oxygenator |
| Manufacturer | Maquet - Getinge QUADROX-i Neonatal Microporous Membrane Oxygenator |
| Models | 92254281, 92262172, 92272396, 11000-J, 92256131, 92272110, 701073392, 92250695, 92261633, 11000, 92245566, 92245287 and 55 more |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | May 10, 2019 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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