7,378 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Foxman Vitrectomy Lens Ring
FDA UDI
OCULAR INSTRUMENTS, INC.·00630238106641·
XPREZZON
FDA Adverse Event
Malfunction
·SPACELABS MEDICAL INC.·Product code MHX·October 2, 2013
REPLY
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code NVZ·October 2, 2015
CSF-VENTRICULAR CATHETER STANDARD 23 CM
FDA Adverse Event
Injury
·MEDTRONICS PS MEDICAL·Product code JXG·September 25, 1996
ASH SPLIT CATHETER
FDA Adverse Event
Malfunction
·MEDCOMP·Product code MPB·October 25, 2002
V-GO DISPOSABLE INSULIN DELIVERY DEVICE
FDA Adverse Event
Death
·ZEALAND PHARMA U.S. INC.·Product code LZG·November 30, 2020
ALIZEA
FDA Adverse Event
Malfunction
·MICROPORT CRM S.R.L.·Product code DXY·December 12, 2024
QUADRA ASSURA CRT-D QUAD RF HV
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NIK·March 7, 2017
HEARTSINE SAMARITAN PAD 360P
FDA Adverse Event
Malfunction
·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·April 8, 2026
V-GO DISPOSABLE INSULIN DELIVERY DEVICE
FDA Adverse Event
Malfunction
·MANNKIND CORPORATION - V-GO·Product code LZG·September 26, 2023
V-GO DISPOSABLE INSULIN DELIVERY DEVICE
FDA Adverse Event
Malfunction
·ZEALAND PHARMA U.S. INC.·Product code LZG·August 10, 2021
HEARTSINE SAMARITAN PAD 350P
FDA Adverse Event
Malfunction
·HEARTSINE TECHNOLOGIES LTD·Product code NSA·May 20, 2026
HEARTSTART MRX - EMS DEFIBRILLATOR
FDA Adverse Event
Other
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·October 5, 2011
CAPSURE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 1997
CAPSURE Z NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DXY·September 9, 2005
CAPSURE SP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 26, 1999
SIGMA 300 DR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code DXY·July 11, 2001
MULTIFUNCTION ELECTRODE
FDA Adverse Event
Other
·CARDIOTRONICS SYSTEM, INC.·Product code LDD·May 22, 1995
THERMOFLOW FILTER PORT
FDA Adverse Event
Malfunction
·ARC MEDICAL·Product code BYD·October 27, 2009
ULTRAVIEW
FDA Adverse Event
SPACELABS HEALTHCARE·Product code DRT·June 12, 2013