8 results
·
17ms
·
Sources: EU EUDAMED, US FDA
SAFETY INJECTION SYSTEM
FDA 510(k)
FDA Class 2
·Dental
SURGISTAR, INC.
FDA UDI
SURGISTAR, INC.·00878799002617·
V-Grip Detachment Controller for use with Hydrocoil Embolic System and MicroPlex Coil System, AZUR Detachment Controller for use with AZUR Peripheral Coil System
FDA 510(k)
FDA Class 2
·Neurology
OPTICATH CENTRAL VENOUS OXIMETRY PROBE WITH SEAL WITH HEPARIN
FDA 510(k)
FDA Class 2
·Cardiovascular
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 11, 2014
SOLETRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·February 15, 2013
TYCO
FDA Adverse Event
Malfunction
·COVIDIEN·Product code GDO·January 5, 2011
Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026