Taiwan FDA registration d8792b2ccacf66d9f295403da31c83c7
Ficon Rotavirus Rapid Test (Unsterilized)
TW: "飛確" 輪狀病毒快速檢驗試劑 (未滅菌)
Registration details
- Analysis ID
- d8792b2ccacf66d9f295403da31c83c7
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PANION & BF BIOTECH INC.
Product details
- Intended Use
- It is limited to the first level of identification scope of the "Poliovirus Serum Reagent (C.3405)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3405 Poliomyelitis virus serum reagent
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 09, 2015
- Expiry Date
- Dec 09, 2025
About this record
Access comprehensive regulatory information for Ficon Rotavirus Rapid Test (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d8792b2ccacf66d9f295403da31c83c7 and manufactured by Baoling Fujin Biotechnology Co., Ltd. Xizhi Plant No. 2 Factory. The authorized representative in Taiwan is PANION & BF BIOTECH INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices