7 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LASER HANDPIECE SHROUD
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515236875·Cottle Osteo, 9mm wide
TAPERFILL FEMORAL HIP STEM 425-31-005_017 425-41-005_019
FDA 510(k)
FDA Class 2
·Orthopedic
BAXTER ARENA HEMODIALYSIS DELIVERY SYSTEM, MODEL 1571278000
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HEARTMATE II SYSTEM CONTROLLER
FDA Adverse Event
Malfunction
·THORATEC CORP·Product code DSQ·November 18, 2010
S-ROM*HEAD FEMORAL COCR 28+12
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JDI·January 25, 2013
ACCU-CHEK ® SPIRIT COMBO
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LZG·July 11, 2014