10 results
·
18ms
·
Sources: EU EUDAMED, US FDA
GIARDIA GUARD
FDA 510(k)
FDA Class 1
·Microbiology
MYOCATH CATOLOG NO. MCK-A
FDA 510(k)ORTHOFIX GALAXY UNYCO DIAPHYSEAL TIBIA KIT
FDA 510(k)
FDA Class 2
·Orthopedic
NA
FDA UDI
Zimmer, Inc.·00889024194427·
NA
FDA UDI
Zimmer, Inc.·00889024194403·
NA
FDA UDI
Zimmer, Inc.·00889024194434·
NA
FDA UDI
Zimmer, Inc.·00889024194410·
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 31, 2014
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·November 21, 2012
MULTI-LUMEN CVC KIT: 3-LUMEN 7 FR X 6IN
FDA Adverse Event
Malfunction
·ARROW INTL., INC.·Product code FOZ·August 27, 2010