9 results
·
16ms
·
Sources: EU EUDAMED, US FDA
105MM ROLL FILM FLUOROGR. CAMERA, #105
FDA 510(k)
FDA Class 2
·Radiology
DELTAVEN
FDA UDI
DELTA MED SPA·08032248381001·Safety IV Catheter in PUR with closed system, Y...
HOLOSCOPE-i
FDA 510(k)
FDA Class 2
·Radiology
POWDER FREE PURPLE NITRILE EXAMINATION GLOVES, NONSTERILE
FDA 510(k)
FDA Class 1
·General Hospital
DELTAVEN Y, Safety I.V. Catheter in Pur with closed system a) REF 3832072 b) REF 3810072 c) REF 3842072 d) REF 3852072
FDA Enforcement
Class II
·Ongoing·Delta Med SpA·August 25, 2021
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORP·Product code MKJ·February 4, 2014
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 11, 2007
3.5MM LOCKING SCREW SLF-TPING W/STARDRIVE RECESS 14MM
FDA Adverse Event
Injury
·SYNTHES, INC.·Product code KTT·October 18, 2012
DELTAVEN Y, Safety I.V. Catheter in Pur with closed system a) REF 3832072 b) REF 3810072 c) REF 3842072 d) REF 3852072
FDA Recall
Open, Classified
·Delta Med SpA Via Guido Rossa 20 Viadana Italy·Product code FOZ·June 21, 2021