This page includes the latest FDA filings for Cordis Europa N V. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
|---|---|---|
CORDIS EUROPA, N.V. | CORDIS AVIATOR PLUS PTA BALLOON DILATATION CATHETER | 2007-05-16 |
CORDIS EUROPA, N.V. | CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER | 2007-03-07 |
CORDIS EUROPA, N.V. | INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED | 2006-04-11 |
CORDIS EUROPA, N.V. | INSCOPE 3-STAGE BALLOON DILATOR | 2005-02-04 |
CORDIS EUROPA N.V. | CORDIS PALMAZ BLUE TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM | 2004-06-21 |
CORDIS EUROPA N.V. | CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS POWERFLEX P3 PTA | 2003-10-02 |
CORDIS EUROPA N.V. | CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM | 2001-08-01 |
| NCAGE Code | H0P66 | CORDIS EUROPA N.V. |
| CAGE Code | H0P66 | CORDIS EUROPA N.V. |