International safety notice
Fabian therapy evolution, números de referencia 121001, 121012; Fabian +nCPAP evolution, número de referencia: 7050.IB, 122001, 7250.IB/122011, 122012; Fabian HFO, números de referencia: 111001, 111001.01, 112001, 113001
Spain / AEMPS · ESP · Jun 10, 2021
Key facts
| Title | Fabian therapy evolution, números de referencia 121001, 121012; Fabian +nCPAP evolution, número de referencia: 7050.IB, 122001, 7250.IB/122011, 122012; Fabian HFO, números de referencia: 111001, 111001.01, 112001, 113001 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Fabian therapy evolution, números de referencia 121001, 121012; Fabian +nCPAP evolution, número de referencia: 7050.IB, 122001, 7250.IB/122011, 122012; Fabian HFO, números de referencia: 111001, 111001.01, 112001, 113001 |
| Manufacturer | Acutronic Medical Systems AG, Suiza |
| Models | AT-01620, AN-01749, AN-01677, IB-00074, AT-01324, 01644, AT-01621, AL-00001, ANXXYY-0853, AT-01499, AT-01327, AT-01305 and 103 more |
| Event type | Safety Notice |
| Date | Jun 10, 2021 |
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