Taiwan FDA registration f34961e1d9dc15a393ef2ae8024252b7

Blood ketone solution (unsterilized)

TW: 暐世血酮品管液(未滅菌)

Taiwan·Risk Class 1·Hsinchu General Factory of Weishi Biotechnology Co., Ltd·Registered May 22, 2019 – May 22, 2029Active

Registration details

Analysis ID: f34961e1d9dc15a393ef2ae8024252b7

Company information

Manufacturer: Hsinchu General Factory of Weishi Biotechnology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Hsinchu General Factory of Weishi Biotechnology Co., Ltd

Product details

Intended Use: Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1660 Quality control materials (analytical and non-analytical)
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: May 22, 2019
Expiry Date: May 22, 2029

About this record

Access comprehensive regulatory information for Blood ketone solution (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f34961e1d9dc15a393ef2ae8024252b7 and manufactured by Hsinchu General Factory of Weishi Biotechnology Co., Ltd. The authorized representative in Taiwan is Hsinchu General Factory of Weishi Biotechnology Co., Ltd.

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