7 results
·
25ms
·
Sources: EU EUDAMED, US FDA
NOVA 8 IONIZED CALCIUM/PH ANALYZER
FDA 510(k)
FDA Class 2
·Clinical Chemistry
LEONE SPA
FDA UDI
LEONE SPA·08033707028802·WEB 1ST MOLAR BANDS n.UL 2
14.5F X 55CM HEMO-FLOW DOUBLE LUMEN CATHETER, MODELS HFS-55, HFT-55
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Ear Pressure Relief Device(Model:ER813B)
FDA 510(k)
FDA Unclassified
·Unknown
UNKNOWN SROM SUPER GRIPPER CUP
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JDI·May 23, 2014
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·October 10, 2012
ACCU-CHEK SPIRIT
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·September 2, 2010