FDA News USFDA Proposes to End Temporary Extension of GUDID’s Grace Period

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Hi Marcelo- I work for a small medical device manufacturer. The GUDID deadline for class I devices under the FDA for products manufactured and labeled after Sept. 24, 2018 is Sept. 24 2020. Our products have 3-year shelf-life. My question is we have inventory of products made after Sept. 24, 2018 on-site and have shipped products that were manufactured and labeled since Sept. 24, 2018 to distributors. Should the products made after Sept. 24, 2018 and shipped out already have had barcodes (since they might be unexpired and on distributors' shelves on compliance date, Sept. 24, 2020)?
Should we be barcoding products we are shipping now for the same reason?
 

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