7 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MODEL 3200 VASCULAR MINI-LAB
FDA 510(k)
FDA Class 2
·Cardiovascular
E.R.C.P. CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MEDIPART XENON BREATHING KIT MP-02XM
FDA 510(k)
FDA Class 2
·Radiology
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 21, 2024
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 5, 2013
MAXTORQUE ZP
FDA Adverse Event
Injury
·ORTHOHELIX SURGICAL DESIGN·Product code HWC·December 27, 2010
PINN CAN BONE SCREW 6.5MMX25MM
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS1219655·Product code NDJ·July 18, 2014