7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SPRING-WOUND EPIDURAL CATHETER
FDA 510(k)
FDA Class 2
·Anesthesiology
RIONET HEARING AID HB-64S
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
DRX-Evolution with Carestream Digital Tomosynthesis
FDA 510(k)
FDA Class 2
·Radiology
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code ITI·March 6, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014
CABLE CUTTER-STANDARD
FDA Adverse Event
Malfunction
·SYNTHES TUTTLINGEN·Product code HXZ·June 25, 2015