Taiwan FDA registration fc49b1beca9282e49dc1d5e01a391111
LIAISON C. difficile GDH Control Set
TW: 禮雅尚困難梭狀桿菌麩胺酸去氫酶品管液
Taiwan·Risk Class 2·MD·DIASORIN INC.·Registered Apr 16, 2019 – Apr 16, 2024ExpiredRegistration details
- Analysis ID
- fc49b1beca9282e49dc1d5e01a391111
- License Form
- Ministry of Health Medical Device Import No. 032410
- Customs Code
- DHA05603241000
Company information
- Manufacturer
- DIASORIN INC.
- Manufacturer Country
- United States
- Authorized Representative
- MEDRICH INSTRUMENT CO., LTD.
Product details
- Intended Use
- This product is a quality control specimen used to monitor the accuracy and precision of the DiaSorin LIAISON C. difficile GDH 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 16, 2019
- Expiry Date
- Apr 16, 2024
About this record
Access comprehensive regulatory information for LIAISON C. difficile GDH 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 fc49b1beca9282e49dc1d5e01a391111 and manufactured by DIASORIN INC.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
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