International safety notice
Dispositivo de inflado basixALPHATM, nos de catálogo IN3130, IN3152, IN3302, IN3802
Spain / AEMPS · ESP · Jun 29, 2021
Key facts
| Title | Dispositivo de inflado basixALPHATM, nos de catálogo IN3130, IN3152, IN3302, IN3802 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Dispositivo de inflado basixALPHATM, nos de catálogo IN3130, IN3152, IN3302, IN3802 |
| Manufacturer | Merit Medical Systems Inc., EEUU. |
| Models | H1993118, H2073249, H1978305, H1896265, 2021-368, H1929107, H1909581, H1978295, H1966490, H2077173, IN3152, H2073248 and 33 more |
| Event type | Safety Notice |
| Date | Jun 29, 2021 |
At a glance
- No Recall
- Yes Field safety notice
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