7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Isolator Synergy EnCapture Ablation System (EMH)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Oticon
FDA UDI
Sbo Hearing A/S·05714464034796·OTICON MORE 1 MINIBTE T C094
Dynamic TiBase
FDA 510(k)
FDA Class 2
·Dental
Kenota 1 Total IgE; Kenota 1 (instrument)
FDA 510(k)
FDA Class 2
·Immunology
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·November 7, 2014
HEART START XL
FDA Adverse Event
Death
·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·August 31, 2011
PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·July 18, 2013