7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KYOKKO SPEC-SERIES INTENSIFY SCREENS-SPEC,SUPER SPEC
FDA 510(k)
FDA Class 1
·Radiology
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC·Product code KWP·December 18, 2014
SOLCO BASLE INTRAOPERATIVE AUTOTTRNSFUS
FDA 510(k)
FDA Class 2
·Anesthesiology
i-Cut
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
SENSAR
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL OPTICS·Product code HQL·February 5, 2013
TUNNELER
FDA Adverse Event
Other
·I-FLOW CORP.·Product code BSO·December 21, 2010
ELLIPSE ST VR, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 18, 2014