International safety notice
Common name: IMPLANTABLE ACTIVE DEVICE PROGRAMMER (IMPLANTABLE ACTIVE DEVICE MANAGEMENT PROGRAM) Sales name: CT900 Doctor Programmer
Japan / PMDA Recalls · JPN · Dec 7, 2022
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | Common name: IMPLANTABLE ACTIVE DEVICE PROGRAMMER (IMPLANTABLE ACTIVE DEVICE MANAGEMENT PROGRAM) Sales name: CT900 Doctor Programmer |
| Manufacturer | Japan Medtronic Co., Ltd. |
| Models | 29U7K6LLR5, EV6SAG9QQY, P5NG7NC7JE, 6XM338H6C6, SM64KLCDGT, MDJJ9W72UT, QWQ7S1LTGW, 4EY9A2KX42, JTEZJPPEF3, 4336JDLZ48, 3DLMVZMAXC, A71200 and 159 more |
| Date | Dec 7, 2022 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
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