International safety notice
fabian HFO, números de referencia: 111001, 111001.01, 112001, 113001; fabian +nCPAP evolution, número de referencia: 122001
Spain / AEMPS · ESP · Nov 23, 2020
Key facts
| Title | fabian HFO, números de referencia: 111001, 111001.01, 112001, 113001; fabian +nCPAP evolution, número de referencia: 122001 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | fabian HFO, números de referencia: 111001, 111001.01, 112001, 113001; fabian +nCPAP evolution, número de referencia: 122001 |
| Manufacturer | Acutronic Medical Systems AG, Suiza. |
| Models | V5.0.X, 5.1.0, FSCA-20-001-FSN, 20-001, CARD-20-001, CARD-20-001.EN, CARD-20-001.ES, V4.X.X, 111001.01, V5.1.X, 1.2.2, TS-AA-027E and 21 more |
| Event type | Safety Notice |
| Date | Nov 23, 2020 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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