8 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MICROETCHER AP
FDA 510(k)
FDA Class 2
·Dental
artegral
FDA UDI
Merz Dental GmbH·D7091970589·anteriors; shade A2 light; mould BOS
C!
FDA 510(k)
FDA Class 2
·Radiology
FILTER, INTRAVENOUS W/AUTO AIR VENT
FDA 510(k)
FDA Class 2
·General Hospital
DEVILBISS
FDA Adverse Event
Injury
·SUNRISE MEDICAL HHG, INC.·Product code CAF·November 8, 2001
PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE
FDA Adverse Event
Malfunction
·MEDELA, INC.·Product code HGX·June 2, 2014
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·UNKNOWN·Product code ITI·February 20, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·January 25, 2011