8 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Peel-Away Introducer Sheath
FDA 510(k)
FDA Class 2
·Cardiovascular
NA
FDA UDI
aap Implantate AG·04042409194108·Extra-articular Radiusplate WSP 2.5, 4/6-Hole, ...
CP Relief Wand Rx - TENS/NMES
FDA 510(k)
FDA Class 2
·Neurology
Swoop® Portable MR Imaging® System (V2)
FDA 510(k)
FDA Class 2
·Radiology
VITALITY 2 DR
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·November 11, 2008
ASR ACETABULAR CUPS 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·September 19, 2011
PINN CAN BONE SCREW 6.5MMX20MM
FDA Adverse Event
Injury
·1219655 DEPUY-RAYNHAM·Product code NDJ·July 30, 2013
BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·Product code FOZ·July 30, 2021