Compliance confusion

Hello all, I have a seller and vendor account. I have some compliance requirements on both accounts but some new categories have popped up and support hasn’t been….supportive. The issue on this post is related to my vendor account.

For background, the nature of my products are scientific/industrial and the general category is LAB_SUPPLY

The below compliance is a new one, I have asked my account manager and he says that he’s unfamiliar with this compliance but that it shouldn’t be attached to my products as they are not to be used for food or drug use/testing. For example, one of the products being flagged for missing this compliance is a nitrile glove. Compliance message below:

“Product packaging and label images, FDA Establishment Registration Number, FDA Device Listing, FDA 510(k) Premarket Notification, and test reports from an ISO 17025-accredited lab”

Does anyone have any insight/experience on this?