8 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ORTHOSCAN, ORTHOSCAN HD
FDA 510(k)
FDA Class 2
·Radiology
MEDIS 5MP1H DUAL-HEAD MEDICAL DIAGNOSTIC DISPLAY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
EXEL SECURETOUCH PTP SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
RENU WITH MOISTURELOC MULTIPURPOSE SOLUTION
FDA Adverse Event
Injury
·BAUSCH & LOMB INCORPORATED·Product code LPN·February 18, 2020
UNKNOWN BIOMET STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·January 21, 2021
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·UNKNOWN·Product code ITI·April 10, 2013
SPRINT FIDELIS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·April 12, 2011
AUTODISC 50 TEST STRIPS
FDA Adverse Event
Injury
·BAYER HEALTHCARE, LLC·Product code NBW·May 23, 2008