6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ANTIBIOTIC NEPHELOMETER
FDA 510(k)
FDA Class 1
·Clinical Chemistry
EIT Cellular Titanium® Lumbar Cage LLIF
FDA 510(k)
FDA Class 2
·Orthopedic
BEAMER ARGON PROBE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
JGRKNT 1.0MM MINI 3-0 NDLS
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBI·April 30, 2014
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 21, 2007
ADVISA DR
FDA Adverse Event
Malfunction
·MEDTRONIC S.A.·Product code NVZ·October 10, 2012