12 results
·
32ms
·
Sources: EU EUDAMED, US FDA
DMA AMYLASE PROCEDURE
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ALILITE CHEST ROLL 12X6X4
FDA UDI
ALIMED, INC.·00733657239591·
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 4, 2019
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 4, 2012
MATCH POINT SYSTEM(TM), SURGICASE CONNECT, MATCH POINT SYSTEM(TM) GUIDES
FDA 510(k)
FDA Class 2
·Orthopedic
RENU MEDICAL REPORCESSED COMPRESSIBLE LIMB SLEEVES
FDA 510(k)
FDA Class 2
·Cardiovascular
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 3, 2024
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 5, 2013
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·May 31, 2013
ALLOCLASSIC SL SCHAFT 6 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·June 23, 2014
ASR ACETABULAR CUPS 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·January 28, 2013
ENDOSTAT ELECTROSURGICAL UNIT
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code KNS·December 17, 2010