10 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CENTRAL VEIN CATHETERIZATION KIT
FDA 510(k)
FDA Class 2
·Cardiovascular
DSQ Alert Internal Control Set IC2
FDA UDI
Elitechgroup Mdx LLC·03661540952555·The DSQ Alert IC2 Probe Mix contains a chemical...
Tobii Dynavox
FDA UDI
TOBII DYNAVOX LLC·07340074601424·SC TABLET PRO, SGD, WITH SNAP + CORE FIRST, STE...
EMS JUMPER II DUAL CHANNEL NEUROMUSCULAR STIMULATOR SYSTEM, MODEL E-188
FDA 510(k)
FDA Class 2
·Physical Medicine
MEGA SOFT REUSABLE PATIENT RETURN ELECTRODE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·May 8, 2014
ENDEAVOR SPRINT RX
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code NIQ·October 23, 2012
OCTRODE 8 ELECTRODE LEAD
FDA Adverse Event
Injury
·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·August 12, 2010
BD PLATE CAMPYLOBACTER SB 100MM
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code JSJ·June 2, 2022
Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems
FDA Enforcement
Class II
·Ongoing·Siemens Medical Solutions USA, Inc.·April 7, 2021