6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ELECTRODE USING PROMEON RG-60 SERIES GEL
FDA 510(k)
FDA Class 2
·Neurology
U.S. TYPE CRUCIATE SLOT BONE SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
CHALLENGE (TM) LIQ THERA DRUG CONTROLS
FDA 510(k)
FDA Class 1
·Clinical Toxicology
COBAS C501
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·June 9, 2014
KNOB F. TARGET DEVICE 40X50MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·November 17, 2010
EONC
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 28, 2012