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FDA Offers Clarity of UDI Application to Kits

08 January 2016

Medical Device Alert

On January 4, 2016, the FDA officially released a draft guidance document Unique Device Identification: Convenience Kits, with further information regarding the Unique Device Identifier (UDI) requirements for labeling and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

The team

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