Taiwan FDA registration 01d9997af8127daaeaa34768d9e2fb7e

Traumatic white blood cell filter/transfusion sleeve

TW: 笙創白血球過濾器/輸血套

Taiwan·Risk Class 2·Shengchuang Co., Ltd.;; Shengte Technology Co., Ltd. Yike Factory·Registered Oct 17, 2011 – Oct 17, 2026Active

Registration details

Analysis ID: 01d9997af8127daaeaa34768d9e2fb7e
Customs Code: DHY00500342809

Company information

Manufacturer: Shengchuang Co., Ltd.;; Shengte Technology Co., Ltd. Yike Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SAFETRAN BIOMEDICAL INC.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.9100 Containers for the collection and disposal of blood and blood components
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: Oct 17, 2011
Expiry Date: Oct 17, 2026

About this record

Access comprehensive regulatory information for Traumatic white blood cell filter/transfusion sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 01d9997af8127daaeaa34768d9e2fb7e and manufactured by Shengchuang Co., Ltd.;; Shengte Technology Co., Ltd. Yike Factory. The authorized representative in Taiwan is SAFETRAN BIOMEDICAL INC..

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