International safety notice
Guider Softip XF Guide Catheter
Swiss / SwissMedic · CHE · Oct 26, 2009
Key facts
| Title | Guider Softip XF Guide Catheter |
|---|---|
| Regulator | Swiss / SwissMedic |
| Country | CHE |
| Brand | Guider Softip XF Guide Catheter |
| Manufacturer | Boston Scientific Corporation |
| Models | H965100510, H965100440, M003101420, 10046, H965100430, 10047, 10063, M003101430, 10043, M003101500, 10146, 10048 and 45 more |
| Event type | Safety Notice |
| Date | Oct 26, 2009 |
| Regulator page | fsca.swissmedic.ch |
At a glance
- No Recall
- Yes Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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