International safety notice
Sistema quirúrgico percutáneo Percuvance®: Eje percutáneo Percuvance® de 29cm y Eje percutáneo Percuvance® de 36cm
Spain / AEMPS · ESP · Jan 29, 2019
Key facts
| Title | Sistema quirúrgico percutáneo Percuvance®: Eje percutáneo Percuvance® de 29cm y Eje percutáneo Percuvance® de 36cm |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistema quirúrgico percutáneo Percuvance®: Eje percutáneo Percuvance® de 29cm y Eje percutáneo Percuvance® de 36cm |
| Manufacturer | Teleflex Medical, EEUU. |
| Models | 73J1700553, 73C1600706, 73J1700074, 73H1700513, 918300462, 73J1600394, 73J1700072, 73G1700577, 73G1700041, 91.822.52.89, 73J1700554, 73F1700585 and 35 more |
| Event type | Safety Notice |
| Date | Jan 29, 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