International safety notice
Dispositivo de embolización Pipeline™ Flex y Pipeline™ Flex con Shield Technology™
Spain / AEMPS · ESP · Sep 17, 2020
Key facts
| Title | Dispositivo de embolización Pipeline™ Flex y Pipeline™ Flex con Shield Technology™ |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Dispositivo de embolización Pipeline™ Flex y Pipeline™ Flex con Shield Technology™ |
| Manufacturer | Micro Therapeutics, Inc. DBA ev3 Neurovascular, EE.UU |
| Models | 2020-534, 28022, 28050, 91.822.52.89, 61981 |
| Event type | Safety Notice |
| Date | Sep 17, 2020 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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