International safety notice
Safety Notice for Guider Softip™ Guide Catheter, Boston Scientific
Germany / BfArM · DEU · Oct 22, 2009
Key facts
| Title | Safety Notice for Guider Softip™ Guide Catheter, Boston Scientific |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Guider Softip™ Guide Catheter, Boston Scientific |
| Manufacturer | Safety Notice for Guider Softip™ Guide Catheter, Boston Scientific |
| Models | 10151, H965100470, 101640, 10147, M003101470, M003100640, 10142, H965100460, M003101420, M003100630, «.S01D, H965100420 and 38 more |
| Date | Oct 22, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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