8 results
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26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ELITE BIOFEEDBACK
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471150744·K-WIRE - SINGLE TROCAR 2.5mm DIA x 150mm
DUREX PLAY WARMER LUBRICANT
FDA 510(k)
FDA Class 1
·General Hospital
Well Lead PVC Urethral Catheter
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·December 30, 2010
PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·February 4, 2013
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVAMEX·Product code IOR·July 17, 2014
DA-400CIII
FDA Adverse Event
Injury
·NAKANISHI INC. (NSK)·Product code EGS·May 26, 2015