International safety notice
Sistema CARDIOHELP-i, modelo 701048012 y UDI-DI 04037691658384 con el cable de conexión de lasonda venosa, L0,23 m, material n.° 701048804 (accesorio) y 701069333 (pieza de repuesto).
Spain / AEMPS · ESP · Dec 15, 2023
Key facts
| Title | Sistema CARDIOHELP-i, modelo 701048012 y UDI-DI 04037691658384 con el cable de conexión de lasonda venosa, L0,23 m, material n.° 701048804 (accesorio) y 701069333 (pieza de repuesto). |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistema CARDIOHELP-i, modelo 701048012 y UDI-DI 04037691658384 con el cable de conexión de lasonda venosa, L0,23 m, material n.° 701048804 (accesorio) y 701069333 (pieza de repuesto). |
| Manufacturer | Maquet Cardiopulmonary GmbH, Alemania. |
| Models | 28521, FSCA-881842, 15-9-2019, 04058863074863, 701048012, 46015, 701048804, 76437, 04037691658384, MARZO-2021, 91.822.52.89, 100152 and 4 more |
| Event type | Safety Notice |
| Date | Dec 15, 2023 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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