International safety notice
MYLA® SOFTWARE V4.7(V4.7.1) - Ref.423270 MYLA® SOFTWARE V4.8(V4.8.1 - V4.8.2) - Ref.423434
Spain / AEMPS · ESP · Sep 23, 2021
Key facts
| Title | MYLA® SOFTWARE V4.7(V4.7.1) - Ref.423270 MYLA® SOFTWARE V4.8(V4.8.1 - V4.8.2) - Ref.423434 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | MYLA® SOFTWARE V4.7(V4.7.1) - Ref.423270 MYLA® SOFTWARE V4.8(V4.8.1 - V4.8.2) - Ref.423434 |
| Manufacturer | bioMérieux, S.A., Francia |
| Models | DL360, V4.8.2, 72418, 45-47, 421993, 28022, 423197, GEN10, 6.184, REF.423270, 5308-1, 51.454 and 13 more |
| Event type | Safety Notice |
| Date | Sep 23, 2021 |
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