204 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MODIFICATION TO BVBLUE
FDA 510(k)
FDA Class 1
·Microbiology
CD HORIZON® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074195476·PROXIMAL SCREW 7.5 X 55, TI
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450141298·
RHIGENE MESACUP2 TEST- SM
FDA 510(k)
FDA Class 2
·Immunology
BAYER DIAGNOSTICS ADVIA CENTAUR TOXOPLASMA IGM ASSAY
FDA 510(k)
FDA Class 2
·Microbiology
ASR ACETABULAR IMPLANT 58
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·April 10, 2013
INSYNC III
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code DXY·April 12, 2011
RIATA ST OPTIM ACTIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026
BIPAP AUTO M-SERIES
FDA Adverse Event
Death
·RESPIRONICS, INC·Product code BZD·July 11, 2012
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 9, 2022
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 14, 2022
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
BIPAP AUTO BIFLEX
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 14, 2022