7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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T-Line® Hernia Mesh
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MEDTRONIC EXTERNAL PULSE GENERATOR (EPG)
FDA 510(k)
FDA Class 2
·Cardiovascular
RADIODEXTER VERSION 1.0, DEXTROSCOPE, MODEL MK10 AND DEXTROBEAM, MODEL MK3
FDA 510(k)
FDA Class 2
·Radiology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 21, 2025
COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·November 18, 2008
HI-TORQUE WHISPER GUIDE WIRE
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code DQX·September 2, 2011
MOTOR EM210 LEGEND STYLUS TOUCH
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC.·Product code EQJ·July 18, 2013