8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HOPE NEBULIZER
FDA 510(k)
FDA Class 2
·Anesthesiology
Life Instruments
FDA UDI
Life Instrument Corporation·M93079804071A0·Suction Tube w/Atraumatic Tip 7FR 4" from bend
Life Instruments
FDA UDI
Life Instrument Corporation·M93079804071AH0·Custom Pediatric Atraumatic Suction W/ Holes 4"...
Smartinhaler
FDA 510(k)
FDA Class 2
·Anesthesiology
BLACKSTONE SFS PARALLEL ROD CONNECTORS
FDA 510(k)
FDA Class 2
·Orthopedic
FRESENIUS 2008K
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 25, 2014
2520274-2013-10533
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code MNI·February 22, 2013
CINCH LEAD ANCHOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION DIV·Product code LGW·February 3, 2011