Taiwan FDA registration 980cb1b61adf55377b1d024ebe90a327

"Yingfang" urine protein reagent (unsterilized)

TW: "瑩芳" 尿蛋白質試劑 (未滅菌)

Taiwan·Risk Class 1·Yingfang Co., Ltd. Taichung Factory·Registered Jul 19, 2011 – Jul 19, 2026Expired

Registration details

Analysis ID: 980cb1b61adf55377b1d024ebe90a327

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 of identification of the "Urine Protein or Albumin (Non-quantitative) Test System (A.1645)" of the Medical Device Classification and Grading Management Measures.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1645 Urine protein or albumin (non-quantitative) testing system
Import Information: Domestic

Dates and status

Registration Date: Jul 19, 2011
Expiry Date: Jul 19, 2026

About this record

Access comprehensive regulatory information for "Yingfang" urine protein 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 980cb1b61adf55377b1d024ebe90a327 and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..

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