3 results
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55ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Recall
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Braemar Manufacturing LLC DL950 Holter Monitor 1285 Corporate Center Dr. Suite 150 Eagan, MN 55121 USA Rx Only
FDA Recall
Terminated
·Braemar Manufacturing, LLC·Product code MWJ·January 22, 2020
Braemar Manufacturing LLC DL900 Holter Monitor 1285 Corporate Center Dr. Suite 150 Eagan, MN 55121 USA Rx Only
FDA Recall
Terminated
·Braemar Manufacturing, LLC·Product code MWJ·January 22, 2020
Monitoring Service Application (MSA). Software to process, analyze, display, and report cardiac events in ECG data received from compatible devices.
FDA Recall
Open, Classified
·Braemar Manufacturing, LLC·Product code DPS·December 18, 2024