23 results · 73ms · Sources: EU EUDAMED, US FDA

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FLEXTIP PLUS CATHETER

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC·Product code BSO·January 2, 2009

ARROW MULTI LUMEN CENTRAL CATHETER TRAY

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code DQO·October 17, 2003

ARROW INTERNATIONAL

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code DQO·July 16, 2003

ARROW INTERNATIONAL

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code DQO·April 25, 2005

ARROW

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code CAZ·June 20, 2005

ARROW - HOWES

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC·Product code DQO·March 13, 2003

ARROW PICC LINE

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code DQO·August 14, 1997

HOWES MULTI-LUMEN CENTRAL VENOUS CATHETERIZATION KIT, 7 FR.

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code DQO·December 5, 1994

ARROW

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC·Product code CAZ·October 3, 2006

CVC KIT: 2-LUMEN 5 FR X 55 CM

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code FOZ·May 1, 2006

ARROW QUAD LUMEN CENTRAL LINE

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code DQO·April 1, 2004

QUAD LUMEN CVC SUPER KIT

FDA Adverse Event
Other ·ARROW INTERNATIONAL INC·Product code DQO·June 25, 2004

ARROWGARD MULTI-LUMEN CVC SUPER KIT

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code DQO·April 30, 2004

ARROW

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code DQO·January 26, 2006

ARROW-HOWES

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code DQO·July 22, 2005

ARROWGARDTRIPLE LUMEN CATHETER

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code DQO·July 26, 2005

ARROW

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code CAZ·July 6, 2005

ARROW

FDA Adverse Event
Other ·ARROW INTERNATIONAL INC.·Product code DYB·January 30, 1998

ARROW

FDA Adverse Event
Other ·ARROW INTERNATIONAL INC·Product code CAZ·May 25, 2001

ARROW GARD

FDA Adverse Event
Other ·ARROW INTERNATIONAL, INC.·Product code DQO·November 28, 1997