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FDA UDI
Uniseal·20744514121007·Nitrile Powder Free Textured Blue Exam Gloves, ...

KAAT II+:E/FE W/REC & HEL 115V

FDA Adverse Event
Malfunction ·ARROW INTL., INC.·Product code DSP·February 28, 2006

KAAT II+: E/FE W/REC & HEL 115V

FDA Adverse Event
Malfunction ·ARROW INTERNATIONAL, INC.·Product code DSP·October 18, 2005

KAAT II+:E/FE W/REC & HEL 115V

FDA Adverse Event
Injury ·ARROW INTL., INC.·Product code DSP·August 9, 2006

BARD MALECOT DRAIN

FDA Adverse Event
Injury ·C.R. BARD, INC.·Product code FEW·January 15, 2004

UNIVERSAL STENT-FIRM 6X26

FDA Adverse Event
Malfunction ·COOK MEDICAL·Product code FEW·August 24, 2015

BARDEX® MALECOT MODEL DRAIN

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FEW·October 18, 2017

BARDEX® MALECOT MODEL DRAIN

FDA Adverse Event
Malfunction ·C. R. BARD, INC.·Product code FEW·December 4, 2017

STAMEY PERCUTANEOUS SUPRAPUBIC CATHETER

FDA Adverse Event
Injury ·COOK UROLOGICAL·Product code FEW·February 17, 1994

BARDEX MALECOT MODEL DRAIN

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FEW·September 29, 2020

MALECOT CATHETER

FDA Adverse Event
Injury ·COOK, INC.·Product code FEW·September 30, 2004

BARD MALECOT DRAIN

FDA Adverse Event
Other ·C.R. BARD, INC.·Product code FEW·September 18, 1997

SILASTIC MALECOT CATHETER

FDA Adverse Event
Injury ·DOW CORNING CORP.·Product code FEW·July 7, 1998

MALECOT CATHETER

FDA Adverse Event
Injury ·COOK MEDICAL·Product code FEW·August 13, 2014

BARDEX MALECOT MODEL DRAIN

FDA Adverse Event
Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FEW·June 9, 2020

BARD UROLOGICAL CATHETER

FDA Adverse Event
Injury ·BARD. C.R. BARD, INC.·Product code FEW·October 6, 2005

BARDEX® MALECOT MODEL DRAIN

FDA Adverse Event
Injury ·C. R. BARD, INC.·Product code FEW·June 3, 2019

BARD MALECOT DRAIN

FDA Adverse Event
Injury ·C.R. BARD, INC.·Product code FEW·November 22, 2006

BARD UROLOGICAL CATHETER

FDA Adverse Event
Injury ·*·Product code FEW·September 27, 2002

1018233-2000-00003

FDA Adverse Event
Injury ·C.R. BARD, INC.·Product code FEW·February 10, 2000