International safety notice
Biosteon IntraLine 5,5 mm, 2 suturas con aguja 3910-200-082 BI200709 I.026 Rev E Biosteon IntraLine 5,5 mm, 3 suturas sin aguja 3910-200-083 BI200709 I.026 Rev E Biosteon IntraLine 6,5 mm, 3 suturas sin aguja 3910-200-086 BI200710 I.026 Rev E
Spain / AEMPS · ESP · Oct 21, 2020
Key facts
| Title | Biosteon IntraLine 5,5 mm, 2 suturas con aguja 3910-200-082 BI200709 I.026 Rev E Biosteon IntraLine 5,5 mm, 3 suturas sin aguja 3910-200-083 BI200709 I.026 Rev E Biosteon IntraLine 6,5 mm, 3 suturas sin aguja 3910-200-086 BI200710 I.026 Rev E |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Biosteon IntraLine 5,5 mm, 2 suturas con aguja 3910-200-082 BI200709 I.026 Rev E Biosteon IntraLine 5,5 mm, 3 suturas sin aguja 3910-200-083 BI200709 I.026 Rev E Biosteon IntraLine 6,5 mm, 3 suturas sin aguja 3910-200-086 BI200710 I.026 Rev E |
| Manufacturer | Biocomposites Ltd, Reino Unido |
| Models | RA20202507720, 28108, 2020-600, 3910-200-083, 2.12-1, 3910-200-086, I.026, RA2020-250772, BI200709, 62309, 38360, 28022 and 4 more |
| Event type | Safety Notice |
| Date | Oct 21, 2020 |
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