International safety notice
Expanded Safety Notice for the PentaRay NAV catheters, Biosense Webster / Johnson & Johnson Medical
Germany / BfArM · DEU · May 22, 2014
Key facts
| Title | Expanded Safety Notice for the PentaRay NAV catheters, Biosense Webster / Johnson & Johnson Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the PentaRay NAV catheters, Biosense Webster / Johnson & Johnson Medical |
| Manufacturer | Expanded Safety Notice for the PentaRay NAV catheters, Biosense Webster / Johnson & Johnson Medical |
| Models | D128202, D128204, D128210, D128201, D128208, D128211, D128205, D128207 |
| Date | May 22, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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