International safety notice
Corrective action for the IntellaTip MiFi™ Open-Irrigated Ablation Catheter, Boston Scientific International S.A.
Germany / BfArM · DEU · Feb 12, 2015
Key facts
| Title | Corrective action for the IntellaTip MiFi™ Open-Irrigated Ablation Catheter, Boston Scientific International S.A. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the IntellaTip MiFi™ Open-Irrigated Ablation Catheter, Boston Scientific International S.A. |
| Manufacturer | Corrective action for the IntellaTip MiFi™ Open-Irrigated Ablation Catheter, Boston Scientific International S.A. |
| Models | M004EPM9620N40, 17237747, 17263604, 17241926, EPM9620K2, 17261879, 17226126, 17233882, 17018928, 17018929, 17223957, 17148152 and 29 more |
| Date | Feb 12, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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