63 results · 72ms · Sources: EU EUDAMED, US FDA

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HEMAQUET EXCEL

FDA Adverse Event
Malfunction ·USCI DIV. C.R. BARD, INC.·Product code DYB·August 29, 1996

PRO-FLO-CATHETER

FDA Adverse Event
Malfunction ·USCI DIV. C.R. BARD, INC.·Product code DQO·August 29, 1996

HEMAQUET EXCEL

FDA Adverse Event
Malfunction ·USCI DIV. C.R. BARD, INC.·Product code DYB·August 29, 1996

BAIM-TURI CATHETER

FDA Adverse Event
Injury ·USCI DIV. C.R. BARD, INC.·Product code DYG·July 10, 1996

HEMAQUET EXCEL

FDA Adverse Event
Malfunction ·USCI DIV. C.R. BARD, INC.·Product code DYB·August 29, 1996

HEMAQUET EXCEL

FDA Adverse Event
Malfunction ·USCI DIV. C.R. BARD, INC.·Product code DYB·August 29, 1996

HEMAQUET EXCEL

FDA Adverse Event
Malfunction ·USCI DIV. C.R. BARD, INC.·Product code DYB·August 29, 1996

HEMAQUET INTRODUCER

FDA Adverse Event
Injury ·USCI DIV. C.R. BARD, INC.·Product code DYB·August 28, 1996

PRO-FLO CATHETER

FDA Adverse Event
Malfunction ·USCI DIV. C.R. BARD, INC.·Product code DQO·August 29, 1996

HEMAQUET EXCEL

FDA Adverse Event
Malfunction ·USCI DIV. C.R. BARD, INC.·Product code DYB·February 18, 1994

STEERABLE GUIDE WIRE

FDA Adverse Event
Malfunction ·USCI DIV., C.R. BARD, INC.·Product code DQX·March 3, 1995

6 FR CATHETER

FDA Adverse Event
USCI DIV. C.R. BARD, INC.·Product code DQO·March 23, 1995

INPUT INTRODUCER

FDA Adverse Event
USCI DIV. C.R. BARD, INC.·Product code DYB·February 10, 1995

WIZARD H

FDA Adverse Event
Malfunction ·USCI DIV C.R. BARD, INC.·Product code MAV·May 22, 1997

PRO-FLO CATHETER

FDA Adverse Event
Malfunction ·USCI DIV., C.R. BARD, INC.·Product code DQO·April 3, 1997

ILLUMEN 8

FDA Adverse Event
Malfunction ·USCI DIV C.R. BARD, INC.·Product code LIT·May 22, 1997

EP XT CATHETER

FDA Adverse Event
Malfunction ·USCI DIV C.R. BARD, INC.·Product code DYG·May 22, 1997

BAIM-TURI CATHETER

FDA Adverse Event
Malfunction ·USCI DIV C.R. BARD, INC.·Product code DRF·May 22, 1997

ARMOD EZ PACK

FDA Adverse Event
Malfunction ·USCI DIV., C.R. BARD, INC.·Product code DQO·June 11, 1997

PRO-FLO CATHETER

FDA Adverse Event
Malfunction ·USCI DIV C.R. BARD, INC.·Product code DQO·May 22, 1997