International safety notice
QUADROX-i/ iD oxigenador con filtro arterial integrado VHK 11000 reservorio de cardiotomía venoso rígido VKMO 10000/11000 reservorio venoso de cardiotomía rígida con oxigenador. Ver referencias afectadas en el anexo I de la nota de aviso de la empresa
Spain / AEMPS · ESP · Apr 3, 2023
Key facts
| Title | QUADROX-i/ iD oxigenador con filtro arterial integrado VHK 11000 reservorio de cardiotomía venoso rígido VKMO 10000/11000 reservorio venoso de cardiotomía rígida con oxigenador. Ver referencias afectadas en el anexo I de la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | QUADROX-i/ iD oxigenador con filtro arterial integrado VHK 11000 reservorio de cardiotomía venoso rígido VKMO 10000/11000 reservorio venoso de cardiotomía rígida con oxigenador. Ver referencias afectadas en el anexo I de la nota de aviso de la empresa |
| Manufacturer | Maquet Cardiopulmonary GmbH, Alemania |
| Models | 70000-USA, 76437, 04058863154435, 31000-J, 04058863154534, 701070388, 04058863153582, 70000-J, 04058863019000, 701070419, 701073019, 701067826 and 156 more |
| Event type | Safety Notice |
| Date | Apr 3, 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