Taiwan FDA registration 744080f0f42e1e0bd2fc845865b4e7ad
“Cepheid” Xpert Check
TW: “賽沛”艾斯柏特儀器檢查組
Taiwan·Risk Class 2·MD·CEPHEID·Registered Apr 08, 2019 – Apr 08, 2024ExpiredRegistration details
- Analysis ID
- 744080f0f42e1e0bd2fc845865b4e7ad
- License Form
- Ministry of Health Medical Device Import No. 032401
- Customs Code
- DHA05603240102
Company information
- Manufacturer
- CEPHEID
- Manufacturer Country
- United States
- Authorized Representative
- PROGRESSIVE GROUP INC.
Product details
- Intended Use
- This product is a system for inspection, verification and hardware testing of 6-color GeneXpert modules.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 08, 2019
- Expiry Date
- Apr 08, 2024
About this record
Access comprehensive regulatory information for “Cepheid” Xpert Check in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 744080f0f42e1e0bd2fc845865b4e7ad and manufactured by CEPHEID. The authorized representative in Taiwan is PROGRESSIVE GROUP INC..
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