8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
ORTHOPHOS 3/ ORTHOPHOS 3C
FDA 510(k)
FDA Class 2
·Dental
OMNI Knee
FDA UDI
Omni Life Science, Inc.·00841690101857·Ultra Tibial Insert CS, Size 6 x 18mm
HEMOCHRON MODEL 8000/FACTOR VI PREMIER COAGULATION
FDA 510(k)
FDA Class 2
·Hematology
EMIT(R) II BARBITURATE ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
SYNCHRON® CK 2 X 400
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code CKA·May 10, 2011
V.A.C. THERAPY
FDA Adverse Event
Injury
·KCI USA INC.·Product code OMP·June 23, 2014
GOBED II
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 30, 2013
SILICONE ADVANCED OPTIC LENS
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code HQL·December 10, 2010