7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CUTANEOUS ELECTRODE
FDA 510(k)
FDA Class 2
·Neurology
SeaSpine Spacer System - Ventura™ NanoMetalene®
FDA UDI
Seaspine Orthopedics Corporation·10889981050153·Ventura NM MIS Inserter, 20 Deg
AIS MODULIFT VBR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ATHENA MULTI-LITE RHEUMATOID FACTOR IGM TEST SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·January 29, 2013
NEXGEN MONOBLOCK LPS TIBIA SIZE: NBR 3
FDA Adverse Event
Injury
·ZIMMER TMT·Product code JWH·December 13, 2010
OT VERIO TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 15, 2014