4 results
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32ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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visby medical COVID-19 Test kit *** An in vitro diagnostic for the qualitative detection of SARS-CoV-2 - Product Usage: The Visby Medical COVID-19 Test is only for use under the Food and Drug Administration s Emergency Use Authorization.
FDA Recall
Terminated
·VISBY MEDICAL INC·Product code QJR·December 5, 2020
visby medical COVID-19 Test kit *** An in vitro diagnostic for the qualitative detection of SARS-CoV-2 - Product Usage: The Visby Medical COVID-19 Test is only for use under the Food and Drug Administration s Emergency Use Authorization.
FDA Enforcement
Class II
·Terminated·VISBY MEDICAL INC·January 20, 2021
ViSi Mobile Chest Sensor (3 lead-wire ECG, AAMI), Catalog No. 93-10014 The ViSi Mobile Monitoring System is intended for use by clinicians and medically qualified personnel for single or multi-parameter vital signs monitoring of adult patients.
FDA Enforcement
Class II
·Terminated·Sotera Wireless, Inc.·August 7, 2013
ViSi Mobile Monitor, Catalog No. 92-10010 The ViSi Mobile Monitoring System is intended for use by clinicians and medically qualified personnel for single or multi-parameter vital signs monitoring of adult patients.
FDA Enforcement
Class II
·Terminated·Sotera Wireless, Inc.·August 7, 2013