8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
DPS 100 MULTIPORT ILLUMINATION SYSTEM (MIS)
FDA 510(k)
FDA Class 2
·Ophthalmic
SeaSpine Spacer System - Pacifica
FDA UDI
Seaspine Orthopedics Corporation·10889981088552·Paddle Distractor, 7mm
Bactiseal Catheters; Bactiseal Barium Striped Catheters; Bactiseal Endoscopic Ventricular Catheter
FDA 510(k)
FDA Class 2
·Neurology
ANGIOVAC CANNULA
FDA 510(k)
FDA Class 2
·Cardiovascular
J-VAC BULB RESERVOIR
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code KOG·January 29, 2013
ATLANTIS SR PRO2 CORONARY IMAGING CATHETER, MODEL 39014
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - FREMONT·Product code DQO·December 20, 2010
SENSOR ENLITE
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OZO·July 14, 2014
BD ULTRA-FINE¿ NANO¿ PEN NEEDLES 4MM (5/32¿) 32G
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·January 4, 2022