Taiwan FDA registration bc29f4ed5dd092724a2c79bbe8b5d19d
"Youkang" group of type A streptococcus detection reagents (unsterilized)
TW: "佑康" A型鏈球菌檢測試劑組(未滅菌)
Registration details
- Analysis ID
- bc29f4ed5dd092724a2c79bbe8b5d19d
- Customs Code
- DHA09402290400
Company information
- Manufacturer
- CEPHEID
- Manufacturer Country
- United States
- Authorized Representative
- PROGRESSIVE GROUP INC.
Product details
- Intended Use
- Classification and grading management method of medical equipment: Streptococcus belongs to the first level identification range of serum reagent (C.3740).
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3740 鏈球菌屬血清試劑
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 23, 2022
- Expiry Date
- Sep 23, 2027
About this record
Access comprehensive regulatory information for "Youkang" group of type A streptococcus detection reagents (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bc29f4ed5dd092724a2c79bbe8b5d19d and manufactured by CEPHEID. The authorized representative in Taiwan is PROGRESSIVE GROUP 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