8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Activmotion Range
FDA 510(k)
FDA Class 2
·Orthopedic
RECAP HIP INSTRUMENTATION
FDA UDI
Biomet Uk Ltd·05019279049943·
M2a-Magnum™
FDA UDI
Biomet Orthopedics, LLC·00887868474804·
CARTO 3 EP NAVIGATION SYSTEM, VERSION 2.0 (W/STANDARD LOCATION PAD),CARTO3 EPNAVIGATION SYSTEM,VERSION 2.0 W/RMT PAD)
FDA 510(k)
FDA Class 2
·Cardiovascular
AMES THERAPY DEVICE
FDA 510(k)
FDA Class 2
·Physical Medicine
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 17, 2013
INSIGNIA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 24, 2011
CAPTURE-R READY SCREEN
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·September 25, 2008