Taiwan FDA registration da01af518088c2d5d3359e854f25e1e9
Ficon Adenovirus Rapid Test Reagent (Unsterilized)
TW: "飛確"腺病毒快速檢驗試劑(未滅菌)
Registration details
- Analysis ID
- da01af518088c2d5d3359e854f25e1e9
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PANION & BF BIOTECH INC.
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management method of medical equipment "adenovirus serum reagent (C.3020)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3020 腺病毒血清試劑
- 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 Adenovirus Rapid Test 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 da01af518088c2d5d3359e854f25e1e9 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