Taiwan FDA registration c09375b9e9964bd2aa0a53427f000ef1
“LIAISON” EHEC Toxins (Non-Sterile)
TW: “禮雅尚” 出血性大腸桿菌檢驗試劑組 (未滅菌)
Taiwan·Risk Class 1·MD·DIASORIN INC.·Registered Sep 06, 2018 – Sep 06, 2023ExpiredRegistration details
- Analysis ID
- c09375b9e9964bd2aa0a53427f000ef1
- License Form
- Ministry of Health Medical Device Import No. 019576
- Customs Code
- DHA09401957602
Company information
- Manufacturer
- DIASORIN INC.
- Manufacturer Country
- United States
- Authorized Representative
- MEDRICH INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "E. coli Serological Reagent (C.3255)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3255 E. coli serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 06, 2018
- Expiry Date
- Sep 06, 2023
About this record
Access comprehensive regulatory information for “LIAISON” EHEC Toxins (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c09375b9e9964bd2aa0a53427f000ef1 and manufactured by DIASORIN INC.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
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