10,000 results
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53ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARCTIC FRONT ADVANCE PRO
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code OAE·March 10, 2021
COSGROVE-EDWARDS ANNULOPLASTY SYSTEM
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code KRH·September 1, 2004
S3 DOUBLE HEAD PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DWB·May 2, 2014
ALLURA XPER FD10/10
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code IZI·August 24, 2011
PLATINIUM
FDA Adverse Event
Malfunction
·MICROPORT CRM S.R.L.·Product code LWS·January 20, 2025
BV 25 GOLD 9"
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code IZL·October 20, 2010
REDIGUARD IAB CATHETER
FDA Adverse Event
Malfunction
·BARD VASCULAR SYSTEM·Product code DSP·October 24, 1996
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 10, 2011
PLATINIUM
FDA Adverse Event
Malfunction
·MICROPORT CRM S.R.L.·Product code NIK·September 9, 2025
T:FLEX INSULIN DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code LZG·December 19, 2019
MEDTRONIC LEAD
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DXY·October 6, 2017
IVENT 201
FDA Adverse Event
Malfunction
·VERSAMED MEDICAL SYSTEMS LTD.·Product code CBK·February 3, 2011
ULYS
FDA Adverse Event
Injury
·MICROPORT CRM S.R.L.·Product code MRM·July 1, 2024
E-LUMINEXX VASCULAR STENT
FDA Adverse Event
Malfunction
·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code NIO·March 22, 2011
CORE SUMEX DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·July 27, 2012
DRILL, AO, STERILE 4,2X180 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code HBE·December 16, 2010
5F STIFF MICRO STICK
FDA Adverse Event
Injury
·MEDCOMP·Product code DQX·May 2, 2014
12.5FX28CM HEMO-CATH
FDA Adverse Event
Malfunction
·MEDCOMP·Product code MSD·September 20, 2013
12.5FX28CM PC HEMO-CATH
FDA Adverse Event
Malfunction
·MEDCOMP·Product code MSD·September 20, 2013
ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION CORPORATION·Product code FRN·August 31, 2011