8 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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XOMED BALL-TIP MONOPOLAR STIMULATOR PROBE
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
ANGIOTEC ZX DIGITAL IMAGE PROCESSOR
FDA 510(k)
FDA Class 2
·Radiology
SherpaPak Lung Preservation System , SherpaPak Liver Transport System
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NOTINGHM SHLDR HUM HEAD 48X17 OFFSET
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWS·January 19, 2016
ASCENT SYSTEM-BEARING
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·December 28, 2016
FERNO MODEL 93-H
FDA Adverse Event
Injury
·FERNO-WASHINGTON, INC.·Product code FPO·February 28, 2013
TERUMO CDI 500 BLOOD PARAMETER MONITOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·February 4, 2011
CAPSURE Z NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO·Product code DTB·August 8, 2014