9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
BARTELS EPSTEIN-BARR VIRUS IGG EIA
FDA 510(k)
FDA Class 1
·Microbiology
BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025
BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025
BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025
TOWERLOX PEDICLE SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
LITE MINERAL OIL
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
PULSE GEN MODEL 102R
FDA Adverse Event
Death
·CYBERONICS, INC.·Product code LYJ·January 18, 2013
PHOENIX INSTRUMENTS
FDA Adverse Event
Malfunction
·EBI, LLC·Product code LXH·December 13, 2010
PROFEMUR(R) TL STEM
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code KWA·July 9, 2014