Taiwan FDA registration b5caa5ebe97d73ef3db40bc1ac1f2391
“Cepheid” Xpert SA Nasal Complete
TW: “賽沛”金黃色葡萄球菌鼻腔檢測試劑組
Registration details
- Analysis ID
- b5caa5ebe97d73ef3db40bc1ac1f2391
- License Form
- Ministry of Health Medical Device Import No. 027370
- Customs Code
- DHA05602737007
Company information
- Manufacturer
- CEPHEID
- Manufacturer Country
- United States
- Authorized Representative
- PROGRESSIVE GROUP INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C1640 Antimicrobial susceptibility test powder
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 15, 2015
- Expiry Date
- Jul 15, 2025
About this record
Access comprehensive regulatory information for “Cepheid” Xpert SA Nasal Complete in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b5caa5ebe97d73ef3db40bc1ac1f2391 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