7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARROW HANDS-OFF THERMO-PACE
FDA 510(k)
FDA Class 2
·Cardiovascular
PRESSURE INFUSOR FOR I.V. BAGS/AUTOINFLATION
FDA 510(k)
FDA Class 2
·General Hospital
TMM MODEL 2500 CAPMONITOR
FDA 510(k)
FDA Class 2
·Anesthesiology
ACCU-CHEK ® MULTICLIX
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·June 25, 2014
PINNACLE MTL INS NEUT40IDX56OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·January 3, 2013
UNK DEEP BRAIN STIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·November 8, 2010
Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system
FDA Enforcement
Class I
·Terminated·CareFusion 303, Inc.·August 12, 2020