9 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ANSPACH MICROMAX SYSTEM
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
XMAX MOTOR
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code ERL·March 31, 2015
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515251816·Aston Face Lift Sci, blunt, curved, 166mm, 6 1/2"
MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TEK-LUBE
FDA 510(k)
FDA Class 1
·Dental
NexGen® Complete Knee Solution
FDA UDI
Zimmer, Inc.·00889024212251·
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 15, 2013
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·July 29, 2014