10 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STRUNG TELFA NON-ADHERENT SPONGE
FDA 510(k)
FDA Class 2
·Neurology
VuePoint
FDA UDI
Nuvasive, Inc.·00887517178916·VuePoint Screw, 5x14mm Cort Occipital
ReLine
FDA UDI
Nuvasive, Inc.·00195377068989·RELINE C Screw, 4.5x14mm MA
LEONE SPA
FDA UDI
LEONE SPA·08033707065890·EXTRAORAL ELASTICS 3/8" 14 oz
Duo Lumbar Interbody Fusion Device
FDA UDI
SPINEOLOGY INC.·M7402904514·Duo, Non-Lordotic, 45 x 14mm
XR MODEL H PHYSIOLOGICAL MONITOR & RECORDING SYS.
FDA 510(k)
FDA Class 2
·Cardiovascular
JYROCHAIR POWER WHEELCHAIR
FDA 510(k)
FDA Class 2
·Physical Medicine
MYNX VASCULAR CLOSURE DEVICE
FDA Adverse Event
Injury
·ACCESSCLOSURE, INC.·Product code MGB·November 22, 2010
ALTRUA
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014
3002 SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·November 30, 2012