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依據衛授食字第1121600286號公告之「醫療器材標籤應刊載單一識別碼規定」規範,醫療器材許可證所有人或登錄者,應於產品市面流通前,至UDID平臺登載DI(產品識別碼)及對應資料;應登載之資訊欄位,不得空白。