72 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LUMENIS VERSACUT TISSUE MORCELLATOR SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
VISIONARY 2000
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CONVERGENCE CERVICAL SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·October 6, 2011
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·July 13, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·July 13, 2017
VPV SYSTEM
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF MEDOS·Product code JXG·January 6, 2014
CODMAN VIPV SYSTEM
FDA Adverse Event
Malfunction
·CODMAN & SHURTLEFF, INC. MEDOS S.A.·Product code JXG·November 5, 2010
CODMAN VPV SYSTEM
FDA Adverse Event
Malfunction
·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·January 11, 2018
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·November 28, 2011
CODMAN VPV SYSTEM
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·October 1, 2016
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·January 7, 2016
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 29, 2012
CODMAN VPV SYSTEM
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·November 12, 2015
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·April 3, 2012
CODMAN VPV SYSTEM
FDA Adverse Event
Malfunction
·CODMAN & SHURTLEFF, INC, MEDOS S.A.·Product code JXG·October 11, 2010
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code OYC·December 15, 2016
CODMAN VPV SYSTEM
FDA Adverse Event
Malfunction
·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·August 16, 2017
CODMAN VPV SYSTEM
FDA Adverse Event
Malfunction
·CODMAN & SHURTLEFF·Product code JXG·January 28, 2015
HS III PROXIMAL SEAL SYSTEM 3.8MM
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code DXC·March 14, 2013