Taiwan FDA registration 3510bfe9b21ab8f9bd0fe2999264adf0
"Saipei" Chlamydomydia/gonorrhoea detection kit
TW: “賽沛”砂眼披衣菌/淋病雙球菌檢測試劑組
Taiwan·Risk Class 2·CEPHEID·Registered Nov 04, 2013 – Nov 04, 2028ActiveRegistration details
- Analysis ID
- 3510bfe9b21ab8f9bd0fe2999264adf0
- Customs Code
- DHA05602553901
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
- Product Type (Level 2)
- C.3390 奈瑟氏菌屬直接血清試劑;; C.3120 披衣菌血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Nov 04, 2013
- Expiry Date
- Nov 04, 2028
About this record
Access comprehensive regulatory information for "Saipei" Chlamydomydia/gonorrhoea detection kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3510bfe9b21ab8f9bd0fe2999264adf0 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