25 results
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48ms
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Sources: EU EUDAMED, US FDA
CARDIOHELP-I, CARDIOHELP Emergency Drive, Accessories
FDA registration
MEDIKOMP GMBH·1 product·🇩🇪 Germany
REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NEXTGEN ALTIUS OCT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Forceps, Biopsy, Electric, Reprocessed
FDA classification
FDA Class 2
·Forceps, Biopsy, Electric, Reprocessed
Appliance, Fixation, Spinal Interlaminal
FDA classification
FDA Class 2
·Appliance, Fixation, Spinal Interlaminal