Today we received final confirmation from FDA that KEWS300 is cleared for sale within the US. The user-centered design and extensive software validations, independently certified to the medical device software standard (ISO62304), allow us to offer this system to US-based customers with real confidence.
Syncrophi Systems
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Where to find us
Syncrophi Systems Ltd
Altar House
Racecourse Business Park
Parkmore
Galway
Ireland
H91 PX6D
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