International safety notice
General names: (1), (2) Residential type X-ray fluoroscopy diagnostic device for Fukuro type circulator, (3) Residential type diagnostic X-ray generation device Brand name: (1) Angiography system Trinias (2) Angiography system BRANSIST safire (3) Diagnostic X-ray high voltage device UD150G-40
Japan / PMDA Recalls · JPN · Nov 5, 2021
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General names: (1), (2) Residential type X-ray fluoroscopy diagnostic device for Fukuro type circulator, (3) Residential type diagnostic X-ray generation device Brand name: (1) Angiography system Trinias (2) Angiography system BRANSIST safire (3) Diagnostic X-ray high voltage device UD150G-40 |
| Manufacturer | Shimadzu Corporation |
| Models | 0161Q80501, 41B24594A001, 41EFCB994001, 40AD5720C001, 41B245D33001, 41E58A969002, 41E584779002, 40AD5732C001, 3M7A12C64001, 3M7A12C42002, 41EFBF39A002, 101H008901 and 370 more |
| Date | Nov 5, 2021 |
| 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