9 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Med-link Reusable Blood Pressure Cuff
FDA 510(k)
FDA Class 2
·Cardiovascular
Neuro Cochlear Implant System
FDA UDI
NEURELEC·03663227003949·SAFETY LINE, CI
MIO ADVANCE
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code FPA·July 20, 2021
ORIGEN REINFORCED DUAL LUMEN CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
ORIGEN BIOMEDICAL DUAL LUMEN 13FR CATHETER
FDA Adverse Event
Injury
·ORIGEN·Product code DWF·June 9, 2015
QUADRA ASSURA CRT-D, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·October 15, 2014
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 17, 2013
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·July 24, 2011