Taiwan FDA registration 205636aeacc2a0c22e7ff763f993be3c

"Yingfang" Staphylococcus aureus latex reagent (unsterilized)

TW: "瑩芳" 金黃色葡萄球菌乳膠試劑 (未滅菌)

Taiwan·Risk Class 1·Yingfang Co., Ltd. Taichung Factory·Registered Apr 29, 2011 – Apr 29, 2026Expired

Registration details

Analysis ID: 205636aeacc2a0c22e7ff763f993be3c

Company information

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

Product details

Intended Use: It is limited to the first-level identification scope of the "Staphylococcus aureus serum reagent (C.3700)" of the classification and grading management measures for medical devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3700 金黃色葡萄球菌血清試劑
Import Information: Domestic

Dates and status

Registration Date: Apr 29, 2011
Expiry Date: Apr 29, 2026

About this record

Access comprehensive regulatory information for "Yingfang" Staphylococcus aureus latex reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 205636aeacc2a0c22e7ff763f993be3c and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..

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