International safety notice
ARveo 8, ARveo, M530 OH y PROvido
Spain / AEMPS · ESP · Sep 19, 2022
Key facts
| Title | ARveo 8, ARveo, M530 OH y PROvido |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | ARveo 8, ARveo, M530 OH y PROvido |
| Manufacturer | Leica Microsystems AG, Suiza. |
| Models | 91.822.52.89, 41-43, 2022.09.13, 5.3.2, 2022-444, 28022, CAPA-HER-MD-22-007, 83618, 08908 |
| Event type | Safety Notice |
| Date | Sep 19, 2022 |
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