Taiwan FDA registration c0fcf13ee7f013c2afac44a11679125b
"Saifei" gene Espert real-time detection PCR analyzer (unsterilized)
TW: "賽飛" 基因艾斯柏特即時偵測PCR分析儀 (未滅菌)
Registration details
- Analysis ID
- c0fcf13ee7f013c2afac44a11679125b
- Customs Code
- DHA04400678902
Company information
- Manufacturer
- CEPHEID
- Manufacturer Country
- United States
- Authorized Representative
- PROGRESSIVE GROUP INC.
Product details
- Intended Use
- Limited to the first level identification range of the microchemical analyzer (A.2170) for clinical use of medical equipment management methods.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2170 Microchemical analyzer for clinical use
- Import Information
- import
Dates and status
- Registration Date
- Jun 05, 2008
- Expiry Date
- Jun 05, 2023
About this record
Access comprehensive regulatory information for "Saifei" gene Espert real-time detection PCR analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c0fcf13ee7f013c2afac44a11679125b 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