8 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
joimax Electrosurgical Instruments
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OXIMETRY INTERFACE KIT
FDA 510(k)
FDA Class 2
·Anesthesiology
FRANKENMAN SURGICAL STAPLERS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 24, 2025
BD ULTRA FINE¿ NANO¿ PEN NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·May 11, 2020
AMT BRIDLE NASAL TUBE RETAINING SYSTEM
FDA Adverse Event
Malfunction
·APPLIED MEDICAL TECHNOLOGY INC·Product code KNT·June 3, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011
PROLIEVE THERMODILITATION KIT
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·September 12, 2008