7 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LIGHT-CORE
FDA 510(k)
FDA Class 2
·Dental
artegral life
FDA UDI
Merz Dental GmbH·D7091993488·anteriors; shade D3; mould UIL
ALOKA PROSOUND ALPHA 6 DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
GlideScope BFlex 3.8 Single-Use Bronchoscope
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code IOR·March 7, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·February 8, 2011
CAPSUREFIX MRI SURESCAN
FDA Adverse Event
Injury
·MPRI·Product code NVN·August 8, 2014