14 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Fusion Robotic Navigation System
FDA 510(k)
FDA Class 2
·Neurology
NA
FDA UDI
Medos International Sàrl·10886705011254·FULLY FLUTED REAMER, STERILE 40 - 130mm (Plus o...
MZ1000
FDA 510(k)
FDA Class 2
·General Hospital
KLS-MARTIN STERNAL PLATING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
DRILL BIT SMALL QUICK COUPLING (SQC) 2.0MM 100/21.5MM
FDA Adverse Event
Malfunction
·GSOURCE, LLC·Product code HTW·September 23, 2024
MAXZERO NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·January 6, 2020
PARADIGM INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code LZG·August 26, 2011
BATTERY 14.8V, 6.3 AH LI-LON BATTERY
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·September 17, 2014
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
ANIMAS CORPORATION·Product code LZG·July 18, 2013
DRILL BIT SMALL QUICK COUPLING (SQC) 2.0MM 100/21.5MM
FDA Adverse Event
Injury
·GSOURCE, LLC·Product code HTW·September 23, 2024
MAXZERO NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·September 2, 2020
DENTAL IMPLANT DRIVER
FDA Adverse Event
Malfunction
·ZIMMER DENTAL·Product code NDP·July 24, 2024
MAXZERO NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·May 8, 2020
MAXZERO NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·May 8, 2020