7 results
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17ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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URIC ACID REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code KNK·April 15, 2011
SYNCHRON CX SYSTEMS URIC ACID (URIC) REAGENT
FDA 510(k)
FDA Class 1
·Clinical Chemistry
PHENOBARBITAL ANALYTICAL TEST PACKS
FDA 510(k)
FDA Class 2
·Clinical Toxicology
The TiBow Expandable Spacer System
FDA 510(k)
FDA Class 2
·Orthopedic
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 21, 2013
AXIEM PORTABLE SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·January 5, 2011
LINOX SMART S DX 65/17
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code NVY·July 31, 2014