8 results
·
21ms
·
Sources: EU EUDAMED, US FDA
SYNCRA TILT OPTION FOR ANGIO DIAGNOST 5
FDA 510(k)
FDA Class 2
·Radiology
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122963·K-WIRE - SINGLE TROCAR 0.9mm DIA x 150mm
MODIFICATION TO NXSTAGE SYSTEM ONE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
STREAMLINE TL SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CHARGING SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 29, 2013
TERUMO CDI 500 BLOOD PARAMETER MONITOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·December 17, 2010
DIMENSION XPAND PLUS WITHOUT HM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·July 17, 2014
Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026