9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Mako Partial Knee Application
FDA 510(k)
FDA Class 2
·Neurology
DANA EMULATING INDICATOR
FDA 510(k)
FDA Class 2
·General Hospital
ALTIVA CLASSIC ACP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BDRV CANN SCW SS P/T DIA4.5X60 MM
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code HWC·March 7, 2017
BDRV CANN SCW SS P/T DIA4.5X52 MM
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code HWC·March 7, 2017
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 5, 2013
ACCU-CHEK RAPID-D LINK INFUSION SET
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code FPA·June 22, 2011
COLLEAGUE VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 24, 2008
BBL Port A Cul tubes with Swabs Sterile Pack, catalog number 221607. For patient sample collection.
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Co.·June 17, 2015