International safety notice
70101.0875 Unidad motriz ROTAFLOW (azul), 70102.2161 Unidad motriz ROTAFLOW (azul),70105.1427 Unidad motriz ROTAFLOW (azul) y MCP0.0952291 Unidad motriz ROTAFLOW (azul, derecha)
Spain / AEMPS · ESP · Dec 11, 2019
Key facts
| Title | 70101.0875 Unidad motriz ROTAFLOW (azul), 70102.2161 Unidad motriz ROTAFLOW (azul),70105.1427 Unidad motriz ROTAFLOW (azul) y MCP0.0952291 Unidad motriz ROTAFLOW (azul, derecha) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | 70101.0875 Unidad motriz ROTAFLOW (azul), 70102.2161 Unidad motriz ROTAFLOW (azul),70105.1427 Unidad motriz ROTAFLOW (azul) y MCP0.0952291 Unidad motriz ROTAFLOW (azul, derecha) |
| Manufacturer | Maquet Cardiopulmonary GmbH, Alemania |
| Models | 04.12.2018, 6.1-6.2, 70101.0875, 70105.1427, 13.12.2018, PRODUCTOS70101.0875, 76437, FSCA-2019-11-11, 91.822.52.89, 910112778, 56059, 28022 and 21 more |
| Event type | Safety Notice |
| Date | Dec 11, 2019 |
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