7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OSTEONICS RESTORATION MONOLITHIC II HIP STEM SERIES
FDA 510(k)
FDA Class 2
·Orthopedic
ELEKTA SYNERGY; ELEKTA SYNERGY S AND XVIR3.5
FDA 510(k)
FDA Class 2
·Radiology
Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing
FDA 510(k)
FDA Class 2
·Orthopedic
BD BBL¿ MGIT¿ OADC ENRICHMENT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·May 13, 2024
CONSULTA CRT-D
FDA Adverse Event
Injury
·IPG MFG SWITZERLAND·Product code NIK·February 9, 2013
CONTAK RENEWAL TR
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NKE·January 7, 2011
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·July 7, 2014