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21/10/20
14:31
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Originally posted by cub40
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Sleepcheck is a class 1 medical device, so can be used as a screening tool and marketed directly to the general public. You can't market a class 2 medical device (Dx) direct to consumers, as it needs medical oversight, so hence no tie-up with HealthEngine. This is a different use case.
A key outcome of the RB collaboration will be understanding the key decision pathways required in the DTC app, to enable Dx to be used as a screening device.
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But isn't HealthEngine seen as "trusted" platform amongst the medical community so if they endorse it as a medical product for remote respiratory consultation, this will be seen as massive by the market.
Last edited by
AlCp :
21/10/20