Taiwan FDA registration 3a4fd597e31a2f347f176ea206b94ac7

"Yingfang" Salmonella serum reagent (unsterilized)

TW: "瑩芳" 沙門氏菌屬血清試劑 (未滅菌)

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

Registration details

Analysis ID: 3a4fd597e31a2f347f176ea206b94ac7

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 "Salmonella Serum Reagent (C.3550)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3550 沙門氏菌屬血清試劑
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" Salmonella serum 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 3a4fd597e31a2f347f176ea206b94ac7 and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..

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