12 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RAPIDONE - MARIJUANA TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Microlife Upper Arm Automatic Digital Blood Pressure Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
KARL STORZ -ENDOSCOPE STERILIZATION TRAYS, MODELS 39402AS, 39301HCTS, 39301BS
FDA 510(k)
FDA Class 2
·General Hospital
AETOS Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556811610·GLENOID REAM BIT XS
AETOS Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556811627·GLENOID REAM BIT S
AETOS Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556811665·GLENOID REAM BIT BP ECCENTRIC
AETOS Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556811634·GLENOID REAM BIT M
AETOS Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556811641·GLENOID REAM BIT L
AETOS Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556811658·GLENOID REAM BIT BP CENTERED
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·March 5, 2013
ADVISA DR MRI SURESCAN
FDA Adverse Event
Injury
·IPG MFG SWITZERLAND·Product code NVZ·August 8, 2014
CAPSUREFIX
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011