230 results
·
79ms
·
Sources: EU EUDAMED, US FDA
PRECISION ENGINEERED PRODUCTS, INC.
FDA registration
PRECISION ENGINEERED PRODUCTS, INC.·4 products·🇹🇼 Taiwan
AIA-360
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·April 4, 2018
AIA-900
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·March 18, 2018
AIA-900
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·February 14, 2018
AIA-600II
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·April 20, 2018
AIA-600II
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·April 9, 2018
AIA-900
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·March 20, 2018
COBE PRECISION BLOOD PUMP
FDA Adverse Event
Other
·COBE CARDIOVASCULAR, INC (NOW SORIN GROUP USA)·Product code DWA·January 25, 2011
VITROS 5,1 FS CHEMISTRY SYSTEM
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·December 16, 2010
AIA-900
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·March 13, 2018
TOSOH HLC-723G8 ANALYZER G8
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·March 28, 2018
AIA-2000
FDA Adverse Event
Malfunction
·TOSOH HI-TEC·Product code KHO·September 8, 2017
VITROS 5600 INTEGRATED SYSTEM
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·August 13, 2021
G8
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·March 28, 2018
AIA-900
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·March 16, 2018
VITROS 5600 INTEGRATED SYSTEM
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·December 4, 2018
AIA-900
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·February 26, 2018
AIA-900
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·March 20, 2018
AIA-360
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·April 5, 2018
TOSOH HLC-723G8 ANALYZER G8
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·March 23, 2018