8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ROSA Partial Knee System
FDA 510(k)
FDA Class 2
·Neurology
Mediflex 3.5mm Laparoscopic Instruments
FDA UDI
FLEXBAR MACHINE CORPORATION·00842102100505·Maxi-Grip Grasper, w/ Flush Port & Locking Hand...
CARESCAPE MONITOR B450
FDA 510(k)
FDA Class 2
·Cardiovascular
INTELEPACS
FDA 510(k)
FDA Class 2
·Radiology
FISCHER CONE BIOP EX MED
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code HGI·July 9, 2020
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·November 13, 2008
ACCUMAX MODEL CU2 MATTRESS PUMP
FDA Adverse Event
Malfunction
·ENCOMPASS THERAPEUTIC SUPPORT SYSTEMS·Product code FNM·August 26, 2011
PERMANENT CAUTERY HOOK INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·July 18, 2013