13 results
·
27ms
·
Sources: EU EUDAMED, US FDA
NMI ANTEGRAD CARDIOPLEGIA CANNULA
FDA 510(k)
FDA Class 2
·Cardiovascular
ZMR®
FDA UDI
Zimmer, Inc.·00889024158061·
ZMR®
FDA UDI
Zimmer, Inc.·00889024158047·
ZMR®
FDA UDI
Zimmer, Inc.·00889024158078·
ZMR®
FDA UDI
Zimmer, Inc.·00889024158054·
C-STEM
FDA UDI
DEPUY INTERNATIONAL LTD·10603295235347·C-STEM CANAL REAMER 13MM
C-STEM
FDA UDI
DEPUY INTERNATIONAL LTD·10603295235354·C-STEM BROACH SZ 1A
6961180
FDA Adverse Event
Malfunction
·October 19, 2017
Oak Ridge Products Sharps Containers
FDA 510(k)
FDA Class 2
·General Hospital
KSEA ROTOCUT G1 ELECTROMECHANICAL MORCELLATOR
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
COYOTE¿ ES
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LIT·February 14, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 11, 2011
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 15, 2014