7 results
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35ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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QUICKPAC II ONE STEP BARBITURATE TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
AssureTech Panel Dip Tests, AssureTech Quick Cup Tests
FDA 510(k)
FDA Class 2
·Clinical Toxicology
KIMBA MINI
FDA 510(k)
FDA Class 2
·Orthopedic
GRANUFLO
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 25, 2014
2520274-2013-10625
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code MNI·February 22, 2013
ECHELON*FLEX60 LONG
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·February 7, 2011
EMBRYO RPLCMNT CATHETER
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code MQF·September 24, 2019