Taiwan FDA registration 750de1402ecc5f82efa4d47904dc54c4
Formosa One Sure Micro-albumin Rapid Test Kit(Non-Sterile)
TW: 台塑生醫迅知尿白蛋白快速檢驗試劑(未滅菌)
Taiwan·Risk Class 1·MD·Formosa Biomedical Technology Co., Ltd. Yilan Factory·Registered May 29, 2019 – May 29, 2024ExpiredRegistration details
- Analysis ID
- 750de1402ecc5f82efa4d47904dc54c4
- License Form
- Ministry of Health Medical Device Manufacturing No. 007780
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FORMOSA BIOMEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Urine Protein or Albumin (Non-quantitative) Test System (A.1645)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1645 Urine protein or albumin (non-quantitative) test system
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 29, 2019
- Expiry Date
- May 29, 2024
About this record
Access comprehensive regulatory information for Formosa One Sure Micro-albumin Rapid Test Kit(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 750de1402ecc5f82efa4d47904dc54c4 and manufactured by Formosa Biomedical Technology Co., Ltd. Yilan Factory. The authorized representative in Taiwan is FORMOSA BIOMEDICAL TECHNOLOGY CORPORATION.
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