13 results
·
27ms
·
Sources: EU EUDAMED, US FDA
IMMUNOCCULT EIA TEST KIT
FDA 510(k)
FDA Class 2
·Hematology
GC Initial™
FDA UDI
Gc America Inc.·J0228711431·GC Initial™ LF Inside IN-43 Sun, 20g
GC Initial™
FDA UDI
Gc America Inc.·15400556705596·GC Initial™ LF Inside IN-43 Sun, 20g
Relievant Medsystems RF Generator
FDA 510(k)
FDA Class 2
·Neurology
BD TRITEST CD3/CD4/CD45, MODEL 340383
FDA 510(k)
FDA Class 2
·Hematology
ACORN 120 STRAIGHT STAIRLIFT
FDA Adverse Event
Death
·ACORN MOBILITY SERVICES LTD·Product code ILK·April 2, 2014
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·October 15, 2010
LARGE NEEDLE DRIVER INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·December 12, 2012
BD TRUCOUNT TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·July 13, 2021
BD TRUCOUNT TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD.·Product code GKZ·July 15, 2021
BD TRUCOUNT¿ ABSOLUTE COUNTING TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·November 30, 2023
BD TRUCOUNT TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·August 24, 2020
BD TRUCOUNT¿ TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·May 2, 2025