Taiwan FDA registration fa0cc804d250d0e14afc4e633c13fa0c

"Yingfang" Aspergillus pylori urease test set (unsterilized)

TW: "瑩芳" 幽門曲狀桿菌尿素酶測試組 (未滅菌)

Taiwan·Risk Class 1·Yingfang Co., Ltd. Taichung Factory·Registered Apr 22, 2011 – Apr 22, 2026Expired

Registration details

Analysis ID: fa0cc804d250d0e14afc4e633c13fa0c

Company information

Manufacturer: Yingfang Co., Ltd. Taichung Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Yingfang Co., Ltd. Taichung Factory

Product details

Intended Use: Limited to the classification and grading management of medical devices, the first level identification range of "Helicobacter serum reagent (C.0003)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.0003 螺旋桿菌屬血清試劑
Import Information: Domestic

Dates and status

Registration Date: Apr 22, 2011
Expiry Date: Apr 22, 2026

About this record

Access comprehensive regulatory information for "Yingfang" Aspergillus pylori urease test set (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fa0cc804d250d0e14afc4e633c13fa0c and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is Yingfang Co., Ltd. Taichung Factory.

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