8 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACTIWATCH
FDA 510(k)
FDA Class 2
·Neurology
PROXIMATE ILS CIRCULAR STAPLES
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.·Product code GAG·June 7, 2006
ECHELON C MRI SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
Unity Total Knee System
FDA 510(k)
FDA Class 2
·Orthopedic
PROXIMATE ILS CIRCULAR STAPLERS
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.·Product code GAG·June 7, 2006
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL MANUFACTURING CORPORATION·Product code MVK·June 26, 2014
CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·February 28, 2013
G2
FDA Adverse Event
Malfunction
·BARD·Product code DTK·February 1, 2011