12 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ENDO PROSTHESIS FEMORAL HEAD
FDA 510(k)
FDA Class 2
·Orthopedic
The Time Machine Series Lasers
FDA 510(k)
FDA Class 2
·Physical Medicine
SYNGO IMAGING VERSION V20A
FDA 510(k)
FDA Class 2
·Radiology
INSYTE AUTOGUARD PNK 20GA X 1.16IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 14, 2019
VERSACARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·May 14, 2014
CAPSURE SP
FDA Adverse Event
Injury
·MPRI·Product code DTB·February 9, 2013
IUNI G2
FDA Adverse Event
Malfunction
·CONFORMIS·Product code HSX·January 4, 2011
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 18, 2020
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 18, 2020
BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 27, 2018
INSYTE-N AUTOGUARD YEL 24GA X .56IN
FDA Adverse Event
Malfunction
·Product code FOZ·September 14, 2021
BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 23, 2019