9 results
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17ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INTERACOUSTICS MODEL AZ26 CLINICAL IMPEDANCE AUDIOMETER
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
ALPHA DUO LAP INSUFFLATOR
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
OSSIOfiber Hammertoe Fixation System/OSSIOfiber Hammertoe Fixation Implant
FDA 510(k)
FDA Class 2
·Orthopedic
INVISION-PLUS
FDA Adverse Event
Malfunction
·RYMED TECHNOLOGIES, LLC·Product code FPA·July 7, 2022
COULTER® ACT DIFF 2 ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC·Product code GKZ·December 7, 2010
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·March 5, 2013
REVO MRI SURESCAN
FDA Adverse Event
Malfunction
·IPG MFG SWITZERLAND·Product code LWP·August 8, 2014
HELIOS H36
FDA Adverse Event
Injury
·CAIRE, INC.·Product code CAW·February 8, 2011
NASAL-AIRE
FDA Adverse Event
Malfunction
·INNOMED TECHNOLOGIES·Product code BYE·January 6, 2003