9 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LOCKBOX
FDA 510(k)
FDA Class 2
·General Hospital
NEWPORT HT70 FAMILY OF VENTILATORS
FDA 510(k)
FDA Class 2
·Anesthesiology
SANSIBAR CPAP SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
HT70 VENTILATOR
FDA Adverse Event
Malfunction
·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·April 13, 2017
NEWPORT
FDA Adverse Event
Malfunction
·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·May 16, 2017
AZO
FDA Adverse Event
Other
·SIEMENS DIAGNOSTICS, INC.·Product code CEN·July 12, 2012
COULTER LH 500 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·June 27, 2014
4 MOTOR ADVANCE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·November 9, 2010
2600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 13, 2012