International safety notice
ORTHO VISION, referencia 6904579, UDI: 10758750012831 y ORTHO VISION® Max referencia and 6904578, UDI: 10758750012848
Spain / AEMPS · ESP · Dec 30, 2022
Key facts
| Title | ORTHO VISION, referencia 6904579, UDI: 10758750012831 y ORTHO VISION® Max referencia and 6904578, UDI: 10758750012848 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | ORTHO VISION, referencia 6904579, UDI: 10758750012831 y ORTHO VISION® Max referencia and 6904578, UDI: 10758750012848 |
| Manufacturer | Ortho Clinical Diagnostics Inc, EEUU. |
| Models | 2022.12.27, 10758750012831, 91.822.52.89, 10758750012848, 28033, 88347, 6904578, 6904579, 10758750012831ORTHO, 28022, J55658, 2022-592 and 2 more |
| Event type | Safety Notice |
| Date | Dec 30, 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