Cordis recalls the Powerflex™ P3 PTA Balloon Dilatation Catheter
2005.05.19
Product group Injections / Infusions / Transfusions / Dialysis
Reference 01111/05
Cordis Europa recalls some lots of the Powerflex™ P3 PTA Balloon Dilatation Catheter. Caused by a narrowed guidewire lumen the insertion of the guide wire may be associated with increased friction.
Cordis recalls the Powerflex™ P3 PTA Balloon Dilatation Catheter , Download_VeroeffentlichtAm_EN