HELP! Have andbody know FDA Test reports 21 CFR PART 801?
Amazon asked me to submit compliance documents for the menstrual cup by submittingTest reports from an ISO 17025 accredited laboratory confirming that each product was assessed to 21 CFR Part 801 (medical device labeling).
But I don't know how I should go about doing this test report and what should be included in the report? Can anyone provide a template for my reference?
Thanks for your help!
HELP! Have andbody know FDA Test reports 21 CFR PART 801?
Amazon asked me to submit compliance documents for the menstrual cup by submittingTest reports from an ISO 17025 accredited laboratory confirming that each product was assessed to 21 CFR Part 801 (medical device labeling).
But I don't know how I should go about doing this test report and what should be included in the report? Can anyone provide a template for my reference?
Thanks for your help!
3 replies
Michelle_Amazon
Hello @Seller_rLOkPGGAr7HDI,
Michelle at Amazon here. I understand that you want to know what you need to submit for menstrual cups in order to list them on Amazon. This help page will guide you through the requirements and how to submit the requested documentation.
I hope this information is helpful.
Regards,
Michelle
