8 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INFRARED EAR THERMOMETER, MODEL KI-8120
FDA 510(k)
FDA Class 2
·General Hospital
Polystar HK
FDA UDI
Merz Dental GmbH·D7091984551·anteriors; shade C4; mould Q 63
Masel
FDA UDI
Ortho Organizers, Inc.·00190707035617·.016 X .016 Lower Retroarch Original Archwires
ENDO TRACHEA TUBE FIXATION
FDA 510(k)
FDA Class 1
·Anesthesiology
DADE FACTOR IX CHROMOGENIC ASSAY
FDA 510(k)
FDA Class 2
·Hematology
DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR
FDA Adverse Event
Death
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 28, 2013
AC-POWERED PATIENT LIFT
FDA Adverse Event
Injury
·INVACARE·Product code FNG·February 2, 2011
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 6, 2014