International safety notice
ORTHO Optix™ Reader para Ortho BioVue (código de producto: 6842223)
Spain / AEMPS · ESP · Apr 27, 2022
Key facts
| Title | ORTHO Optix™ Reader para Ortho BioVue (código de producto: 6842223) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | ORTHO Optix™ Reader para Ortho BioVue (código de producto: 6842223) |
| Manufacturer | Ortho Clinical Diagnostics Inc, Reino Unido |
| Models | 10758750032853, SOFTWARE1.0.0, 79035, 28033, 91.822.52.89, 6842223, 1.0.0, 2022-197, 28022 |
| Event type | Safety Notice |
| Date | Apr 27, 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