8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HLS KNEETEC SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
N/A
FDA UDI
GEORGE TIEMANN & CO.·B58280940130·ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
Ambassador
FDA UDI
Choice Spine, LP·10885862263070·
H & W HOSPITAL ETHYLENE OXIDE STERILIZER CONTROL SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
IMPLEX CONTINUUM KNEE SYSTEM-PATELLAR COMPONENTS, MODEL 04-XX-YYYYY
FDA 510(k)
FDA Class 2
·Orthopedic
URETEX SUPPORT PP KIT X1
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code FTL·April 5, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·September 16, 2014
CONTOUR
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC·Product code NBW·April 20, 2011