8 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACCUGUIDE MUSCLE INJECTION MONITOR
FDA 510(k)
FDA Class 2
·Neurology
MAINFRAME 8253001 NIM RESPONSE 3.0
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC·Product code ETN·November 7, 2013
BONGROS HA
FDA 510(k)
FDA Class 2
·Dental
Tablo Hemodialysis System, Tablo Cartridge
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TRILOGY LONGEVITY LINER STANDARD 32 MM I.D.
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·December 6, 2024
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 5, 2013
ASPHERE M SPEC 12/14 44 +1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWA·February 8, 2011
CAPSURE SP
FDA Adverse Event
Injury
·MPRI·Product code DTB·August 8, 2014