International safety notice
Desfibrilador automático implantable (DAI) CobaltTM XT DR DF4 MRI SureScan, números de modelo DDPA2D4 y DTPA2D4; Desfibrilador con terapia de resincronización cardíaca (TRC-D) CobaltTM XT HF DF1 MRI SureScan, número de modelo DTPA2D1
Spain / AEMPS · ESP · Sep 1, 2020
Key facts
| Title | Desfibrilador automático implantable (DAI) CobaltTM XT DR DF4 MRI SureScan, números de modelo DDPA2D4 y DTPA2D4; Desfibrilador con terapia de resincronización cardíaca (TRC-D) CobaltTM XT HF DF1 MRI SureScan, número de modelo DTPA2D1 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Desfibrilador automático implantable (DAI) CobaltTM XT DR DF4 MRI SureScan, números de modelo DDPA2D4 y DTPA2D4; Desfibrilador con terapia de resincronización cardíaca (TRC-D) CobaltTM XT HF DF1 MRI SureScan, número de modelo DTPA2D1 |
| Manufacturer | Medtronic Inc., Estados Unidos |
| Models | RTH600707S, 61851, 2020-509, DTPA2D4, RSM601556S, RTH600702S, RSM601555S, DTPA2D1, RTG600743S, DDPA2D4, RSM601547S, FA925 and 9 more |
| Event type | Safety Notice |
| Date | Sep 1, 2020 |
At a glance
- No Recall
- Yes 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