10,000 results
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Sources: EU EUDAMED, US FDA
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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