8 results
·
28ms
·
Sources: EU EUDAMED, US FDA
ADENOVIRUS ANTIGEN DETECTION ELISA TEST SYSTEM
FDA 510(k)
FDA Class 1
·Microbiology
Fresh Cells
FDA UDI
DIAGNOSTIC HYBRIDS, INC.·30014613335092·R-MIX TOO MW PLATES 24W6F
NON-STERILE, POWDER FREE, PINK LATEX EXAMINATION GLOVES WITH CHERRY FLAVOUR AND PROTEIN LABELING CLAIMS (50 UG OR LESS)
FDA 510(k)
FDA Class 1
·General Hospital
Ingenuity TF
FDA 510(k)
FDA Class 2
·Radiology
SMART PERFUSION PACK: APEX MBR FMC/MID WEST REG LEXINGTON, KY
FDA Adverse Event
Injury
·Product code DTZ·September 11, 2007
PINN MAR +4 10D 28IDX48OD
FDA Adverse Event
Injury
·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LPH·February 21, 2013
PFCSIG FLUT FEMROD 5DG14X125MM
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·January 26, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·July 31, 2014