International safety notice
Flexima™ Duodenal Bend Stent Biliar con Sistema Introductor, modelos M00539220 y M00539210
Spain / AEMPS · ESP · Jan 9, 2019
Key facts
| Title | Flexima™ Duodenal Bend Stent Biliar con Sistema Introductor, modelos M00539220 y M00539210 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Flexima™ Duodenal Bend Stent Biliar con Sistema Introductor, modelos M00539220 y M00539210 |
| Manufacturer | Boston Scientific Corporation, EEUU |
| Models | «HOSPITAL_NN1NE», 28042, M00539210, LOTE22960202, 22960201, 08714729162520, 92338453-FA, 91.822.52.89, M00539220, 28022, 22960202, YM00539210 and 3 more |
| Event type | Safety Notice |
| Date | Jan 9, 2019 |
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