8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
KT AIR BED
FDA 510(k)
FDA Class 2
·General Hospital
artegral
FDA UDI
Merz Dental GmbH·D7091970468·anteriors; shade BL1; mould BL
UNIPOLAR LEAD CONFIGURATION CONDUCTOR
FDA 510(k)
FDA Class 3
·Cardiovascular
IMPLANT SCIENCES CORP. MODEL HDR 4454
FDA 510(k)
FDA Class 2
·Radiology
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·June 29, 2017
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 20, 2013
LINA LOOP
FDA Adverse Event
Malfunction
·LINA MEDICAL POLSKA SP. Z.O.O·Product code KNF·January 19, 2011
ACCU-CHEK ® AVIVA COMBO
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·July 31, 2014