FDA Offers Clarity of UDI Application to Kits By Jodi Scott & Lina Kontos on February 9, 2016 Email this postTweet this postLike this postShare this post on LinkedIn On January 4, 2016, FDA officially released a draft guidance document Unique Device Identification: Convenience Kits, with further information regarding the Unique Device Identifier (UDI) requirements for labeling and data submission for kits. Read More: FDA Offers Clarity of UDI Application to Kits