23 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Deltaven Fast Flash Closed I.V. Catheter Systems
FDA 510(k)
FDA Class 2
·General Hospital
DESS dental smart solutions
FDA UDI
TERRATS MEDICAL SL.·08435457200802·Conic OSS
939UDX URINE PATHOLOGY SYSTEM
FDA 510(k)
FDA Class 2
·Hematology
TYCHE PEDICLE SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 28, 2025
TRANSVENE RV
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code LWS·August 8, 2014
TRANSVENE RV
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code LWS·August 8, 2014
TRANSVENE RV
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code LWS·August 8, 2014
TRANSVENE RV
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code LWS·August 8, 2014
NOVAMAX LINK GLUCOSE MONITOR
FDA Adverse Event
Other
·NOVA BIOMEDICAL CORPORATION·Product code NBW·October 10, 2008
PRECISION XTRA
FDA Adverse Event
Injury
·Product code NBW·August 11, 2011
PULSE GEN MODEL 103
FDA Adverse Event
Injury
·CYBERONICS INC·Product code LYJ·July 1, 2013
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·September 25, 2024
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·July 13, 2023
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·May 23, 2024
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·June 7, 2024
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·November 28, 2024
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·October 31, 2023
MEDTROINIC GEM
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DXY·June 10, 2014
TRANSVENE RV
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code LWS·June 10, 2014