6 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MANUAL RESUSCITATOR WITH ACE
FDA 510(k)
FDA Class 2
·Anesthesiology
ClearLink Controlled Phototherapy Equipment
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OSTEORAPTOR SUTURE ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FPO·January 25, 2013
COBAS 6000 C501 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JHS·February 9, 2011
ACCESS ACCUTNI+3 REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·August 5, 2014