International safety notice
Common Name: Implant Active Device Management Program Sales name: CT900 Doctor Programmer
Japan / PMDA Recalls · JPN · Jul 29, 2022
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | Common Name: Implant Active Device Management Program Sales name: CT900 Doctor Programmer |
| Manufacturer | Japan Medtronic Co., Ltd. |
| Models | 7C9QMNSWAD, BT4G88MJEN, K8B25KH7VY, FUB6JSEDZW, VJ4Y8PXBJJ, GML79FXH8Y, 7DQ545G7K9, TST6Y9CEGV, EWAG29GSJ4, JPRV3FJ8HT, NECPRS7UJS, MMZ2XTLSZ9 and 334 more |
| Date | Jul 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