9 results
·
20ms
·
Sources: EU EUDAMED, US FDA
VECTRA MAGNETIC RESONANCE SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471123823·K-WIRE - DOUBLE TROCAR 1.6mm DIA x 75mm
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471121928·K-WIRE - DOUBLE TROCAR 1.6mm DIA x 125mm
CODMAN BACTISEAL EVD CATHETER SET
FDA 510(k)
FDA Class 2
·Neurology
INTRABEAM SYSTEM WITH INTRABEAM SPHERICAL APPLICATORS
FDA 510(k)
FDA Class 2
·Radiology
INVISION-PLUS
FDA Adverse Event
Malfunction
·RYMED TECHNOLOGIES, LLC·Product code FPA·July 7, 2022
ACHIEVA VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·May 29, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 10, 2013