26 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
DRYSTAR, MODEL 4500M
FDA 510(k)
FDA Class 2
·Radiology
LGN PS HIGH FLEX XLPE SZ 1-2 13MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·August 9, 2017
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304137411·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304137473·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304137497·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304137459·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304137374·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304137350·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304137398·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304137336·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304137435·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304137299·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304137312·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304137510·
ACETABULAR PLATES
FDA 510(k)
FDA Class 2
·Orthopedic
THE NIMBLE ROCKET POWERED WHEELCHAIR
FDA 510(k)
FDA Class 2
·Physical Medicine
LGN PS HIGH FLEX XLPE SZ 1-2 13MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·August 9, 2017
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FPO·February 26, 2013
ASR UNI FEMORAL IMPL SIZE 47
FDA Adverse Event
Injury
·DEPUY INT'L., LTD.·Product code KWA·February 24, 2011
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·March 11, 2008