11 results
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36ms
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Sources: EU EUDAMED, US FDA
MODIFICATION TO COLLAWOUND DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
SOLIDEA
FDA UDI
CALZIFICIO PINELLI SRL·08300496070269·SOCKS FOR YOU BAMBOO CAREZZA, SIZE L, CAPPUCCIN...
BELLEGLASS HP OPACEOUS DENTIN
FDA 510(k)
FDA Class 2
·Dental
PROCERA ALLCERAM BRIDGE MATERIAL
FDA 510(k)
FDA Class 2
·Dental
SERVICE, CCU, HIGH DEF, 560P, 2NDGEN
FDA Adverse Event
Malfunction
·SMITH & NEPHEW, INC.·Product code GCJ·May 9, 2016
IMPRESS PERIPHERAL CATHETER
FDA Adverse Event
Malfunction
·MERIT MEDICAL SYSTEMS, INC·Product code DQO·June 28, 2017
WAVEWRITER ALPHA? 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·March 21, 2025
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·April 16, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code MDS·April 19, 2011
GE OEC 9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 9, 2008
Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.
FDA Enforcement
Class II
·Terminated·Belmont Instrument Corporation·October 24, 2012