Pure Global

“Cepheid” Xpert SA Nasal Complete - Taiwan Registration b5caa5ebe97d73ef3db40bc1ac1f2391

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 Database
Powered by Pure Global AI
89,000+ Devices
b5caa5ebe97d73ef3db40bc1ac1f2391
Registration Details
Taiwan FDA Registration: b5caa5ebe97d73ef3db40bc1ac1f2391
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Cepheid” Xpert SA Nasal Complete
TW: “賽沛”金黃色葡萄球菌鼻腔檢測試劑組
Risk Class 2
MD

Registration Details

b5caa5ebe97d73ef3db40bc1ac1f2391

Ministry of Health Medical Device Import No. 027370

DHA05602737007

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

C Immunology and microbiology devices

C1640 Antimicrobial susceptibility test powder

Imported from abroad

Dates and Status

Jul 15, 2015

Jul 15, 2025