Taiwan FDA registration d82012f08aa38b6dba47fbdbbb767f90
LIAISON C. difficile Toxins A&B Control Set
TW: 禮雅尚困難梭狀桿菌毒素A與B品管液
Taiwan·Risk Class 2·MD·DIASORIN INC.·Registered Apr 30, 2019 – Apr 30, 2024ExpiredRegistration details
- Analysis ID
- d82012f08aa38b6dba47fbdbbb767f90
- License Form
- Ministry of Health Medical Device Import No. 032415
- Customs Code
- DHA05603241500
Company information
- Manufacturer
- DIASORIN INC.
- Manufacturer Country
- United States
- Authorized Representative
- MEDRICH INSTRUMENT CO., LTD.
Product details
- Intended Use
- This product is used to monitor the accuracy and precision of the LIAISON C. difficile Toxins A&B Assay.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 30, 2019
- Expiry Date
- Apr 30, 2024
About this record
Access comprehensive regulatory information for LIAISON C. difficile Toxins A&B Control Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d82012f08aa38b6dba47fbdbbb767f90 and manufactured by DIASORIN INC.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
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