Taiwan FDA registration 141d4c30dc78af9d3029e0c4ff6cd51a
Formosa FOB Test
TW: 台塑生醫糞便潛血試劑
Taiwan·Risk Class 2·MD·Formosa Biomedical Technology Co., Ltd. Yilan Factory·Registered Sep 01, 2014 – Sep 01, 2024ExpiredRegistration details
- Analysis ID
- 141d4c30dc78af9d3029e0c4ff6cd51a
- License Form
- Ministry of Health Medical Device Manufacturing No. 004709
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FORMOSA BIOMEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- For in vitro quantitative analysis of human heme content in human feces in clinical experiments.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B6550 Occult blood test
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 01, 2014
- Expiry Date
- Sep 01, 2024
About this record
Access comprehensive regulatory information for Formosa FOB Test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 141d4c30dc78af9d3029e0c4ff6cd51a and manufactured by Formosa Biomedical Technology Co., Ltd. Yilan Factory. The authorized representative in Taiwan is FORMOSA BIOMEDICAL TECHNOLOGY CORPORATION.
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