International safety notice
Software update of the MRI-Patient Monitoring Systems Precess 3160 from Invivo
Germany / BfArM · DEU · Jun 18, 2007
Key facts
| Title | Software update of the MRI-Patient Monitoring Systems Precess 3160 from Invivo |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Software update of the MRI-Patient Monitoring Systems Precess 3160 from Invivo |
| Manufacturer | Software update of the MRI-Patient Monitoring Systems Precess 3160 from Invivo |
| Models | 32826, 407-206-9568, 1407-275-3220, 12601, 1-407-249-2022, 221-1593, 1-800-331-3220 |
| Date | Jun 18, 2007 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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