11 results
·
25ms
·
Sources: EU EUDAMED, US FDA
BETA-CAP
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CoRoent
FDA UDI
Nuvasive, Inc.·00887517810113·Interlock II, 14x17x14mm 20°
n.a.
FDA UDI
Karl Storz GmbH & Co. KG·04048551198599·Injection Cannula, 20 cm, 3x
BIOCORE II TC
FDA UDI
HISTO S.A.·G635771420·Biopsy Needles Biocore II TC
Performa®
FDA UDI
Merit Medical Systems, Inc.·00884450000397·
1717SCC_127um and 1717SCC_140um
FDA 510(k)
FDA Class 2
·Radiology
CHAMELEON FIXATION SYSTEM
FDA 510(k)
FDA Unclassified
·Unknown
COGNIS
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·April 24, 2014
CORE IMPACTION DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·September 28, 2012
VENTAK PRIZM
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 27, 2010
GE Healthcare, Compact Airway Modules E-CO, E-COV, E-COVX, E-CAiO, E-CAiOV and E-CAiOVX. The Datex-Ohmeda S/5MT Compact Airway Module, E-CAiOVX family is used for monitoring hospital patients respiration, ventilation, and gas exchange status.
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·June 25, 2014