2 results
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20ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017, 6660E-PA00014, 6660E-PA00012, 6660E-PA00011, 6660E-PA00018, 6660E-PA00015, 6660E-PA00020, Q6660E-PA00011, 6660E-PA00021, 6660E-PA00016, 6660E-PA00019, Q6660E-PA00018, 6660E-PA00010, Q6660E-PA00010, Q6660E-PA00021, Q6660E-PA00012, 6660E-PA00030, 6660E-PA00041, 6660E-PA00035, 6660E-PA00032, 6660E-PA00031. Software Versions: 1.04.00.01, 01.05.00.01, 01.06.00.01, and 01.06.01.01 The patient monitor is intended for monitoring, displaying, reviewing, storing, alarming and transferring of multiple physiological parameters.
FDA Recall
Open, Classified
·Mindray DS USA, Inc. dba Mindray North America·Product code MHX·August 15, 2025
WorkMate Claris v.1.2 Upgrade Kits, Model Numbers H800007 and H800012
FDA Recall
Terminated
·Abbott Laboratories Inc. (St Jude Medical)·Product code DQK·May 5, 2021