Lot recall of PRECISE PRO RX Nitinol Stent System, Cordis
2016.05.30
Product group Non-active implants - special implants
Reference 03895/16
For further information as well as details concerning the device please see the enclosed Advisory Notice of the manufacturer.
Lot recall of PRECISE PRO RX Nitinol Stent System, Cordis , Download_VeroeffentlichtAm_EN