88 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Fukuda Denshi DynaScope Model DS-8000 Series Patient Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04064984699526·GENUMEDI PSS BLUE, SIZE O
RUSCH
FDA UDI
TELEFLEX INCORPORATED·14026704629654·Rusch Polaris FO Blade, Miller 3
RUSCH
FDA UDI
TELEFLEX INCORPORATED·14026704711779·Rusch Polaris FO Blade, Miller 3
LMA PROSEAL, REU, SIZE 3 (150030)
FDA Adverse Event
Malfunction
·THE LARYNGEAL MASK COMPANY·Product code CAE·October 2, 2017
LMA PROSEAL, REU, SIZE 3 (150030)
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAE·October 3, 2017
LMA PROSEAL, REU, SIZE 3 (150030)
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL ASIA PTE LTS·Product code CAE·January 6, 2014
LMA PROSEAL, REU, SIZE 3 (150030)
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAE·November 6, 2018
LMA PROSEAL, REU, SIZE 3 (150030)
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAE·November 2, 2018
LMA PROSEAL, REU, SIZE 3 (150030)
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAE·May 16, 2017
LMA PROSEAL, REU, SIZE 3 (150030)
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAE·September 26, 2017
LMA PROSEAL, REU, SIZE 3 (150030)
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAE·August 8, 2017
LMA PROSEAL, REU, SIZE 3 (150030)
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAE·February 26, 2018
LMA PROSEAL, REU, SIZE 3 (150030)
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAE·February 27, 2018
LMA PROSEAL, REU, SIZE 3 (150030)
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAE·June 20, 2018
POWERX
FDA UDI
SOLTA MEDICAL·00816995021599·ACCESSORY KIT, MANGUBAT, PWX
PIPELINE
FDA UDI
Micro Therapeutics, Inc.·00847536009943·FA-71500-30 PIPELINE EMB DEVICE
Pipeline
FDA UDI
Micro Therapeutics, Inc.·00836462014992·Embolization Device
PIPELINE
FDA UDI
Micro Therapeutics, Inc.·00847536009929·FA-71500-30 PIPELINE EMB DEVICE
AVANTAGE CMNTD SHELL SS 44MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·July 22, 2025