Taiwan FDA registration d56ff030674cdc2c6492fc48b35fe44e
〝IF〞MANUAL POLYBRENE REAGENT CONTROL
TW: 〝瑩芳〞凝聚胺聚合試劑品管液
Taiwan·Risk Class 2·MD·Yingfang Co., Ltd. Taichung Factory·Registered May 10, 2019 – May 10, 2024ExpiredRegistration details
- Analysis ID
- d56ff030674cdc2c6492fc48b35fe44e
- License Form
- Ministry of Health Medical Device Manufacturing No. 006296
Company information
- Manufacturer
- Yingfang Co., Ltd. Taichung Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- IN FUNG CO., LTD.
Product details
- Intended Use
- This product is the quality control liquid of "Yingfang" agglutation amine polymerization reagent.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 10, 2019
- Expiry Date
- May 10, 2024
About this record
Access comprehensive regulatory information for 〝IF〞MANUAL POLYBRENE REAGENT CONTROL in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d56ff030674cdc2c6492fc48b35fe44e and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..
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