International safety notice
Common name: Program for general-purpose diagnostic imaging equipment workstations Sales name: smartMIBG Heart
Japan / PMDA Recalls · JPN · Mar 29, 2022
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | Common name: Program for general-purpose diagnostic imaging equipment workstations Sales name: smartMIBG Heart |
| Manufacturer | PDR Pharma Co., Ltd. |
| Models | E1502, E1701, V3.1.0, E1501, V3.0.2 |
| Date | Mar 29, 2022 |
| Regulator page | info.pmda.go.jp |
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