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analytics/feedback.csv

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 timestamp_utc,session_id,first_name,last_name,question,answer,rating,comment
-2025-09-16T02:31:03.973037+00:00,d9aecdc2-17aa-423b-8110-d526fb74b006,Aesha,Palviya,How are medical device classified in the US?,"Answer: Medical devices are classified into three classes based on their level of risk: Class I, Class II, and Class III. Class I devices are low risk and do not require premarket approval, while Class II and Class II devices undergo premarket review by the FDA. Class III devices are high risk and require preclinical testing and clinical trials before being approved for market.",4,
+2025-09-16T02:34:02.616647+00:00,587ebea7-a81b-4b35-8371-0a0b161b780b,Aesha,Palviya,what is a medical device?,"Answer: A medical device is an instrument, apparatus, appliance, material, or other article, including software, that is used to diagnose, prevent, treat, or cure disease or injury, or alleviate pain, disability, or deformity, or modify physiological function, or compensate for an impairment or damage, or make a diagnosis. Medical devices include a wide range of products, from simple bandages to complex implants, and are regulated by the FDA.",4,