7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INNOVASIVE DEVICES MENISCAL SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
KOWA GENESIS-D
FDA 510(k)
FDA Class 2
·Ophthalmic
Aptima Combo 2 Assay (Panther System)
FDA 510(k)
FDA Class 2
·Microbiology
CLEARVIEW UTERINE MANIPULATOR
FDA Adverse Event
Injury
·CLINICAL INNOVATIONS, LLC·Product code LKF·June 11, 2024
IMPAX CV DICOMSTORE WITH MEDIA PURGE DAEMON (MPD)
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP.·Product code LLZ·February 27, 2013
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·February 7, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 5, 2014