International safety notice
Medtronic Inc. Synchromed II - MRT-suunised SynchroMed infusioonisüsteemi jaoks
Estonia / EMDDB · EST · Nov 1, 2023
Key facts
| Title | Medtronic Inc. Synchromed II - MRT-suunised SynchroMed infusioonisüsteemi jaoks |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Medtronic Inc. Synchromed II |
| Manufacturer | MEDTRONIC INC SYNCHROMED II |
| Models | 00643169384125, 00763000421809, 00763000122744, 00763000122850, 00763000689582, 00643169384163, 00763000689643, 00763000421762, 00643169700956, 00643169999923, 00763000122799, 00613994518781 and 154 more |
| Date | Nov 1, 2023 |
| Regulator page | terviseamet.ee |
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