9 results
·
28ms
·
Sources: EU EUDAMED, US FDA
OPUS SMARTSTITCH SUTURE DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
POWDERED LATEX EXAM GLOVES, PINK, WITH/WITHOUT STRAWBERRY SCENT, PROTEIN LABELING
FDA 510(k)
FDA Class 1
·General Hospital
POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE
FDA 510(k)
FDA Class 1
·General Hospital
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 9, 2022
PLATE BD CHROMAGAR O-157 20 EA
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JSI·August 10, 2021
PLATE BD CHROMAGAR O-157 20 EA
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JSI·August 10, 2021
OBTAPE TRANSOBTURATOR SLING
FDA Adverse Event
Injury
·MENTOR WORLDWIDE LLC·Product code OTN·April 12, 2013
CORAIL2 NON COL HO SIZE 12
FDA Adverse Event
Injury
·DEPUY FRANCE SAS·Product code KWA·September 9, 2014
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·April 27, 2011