Taiwan FDA registration 363068c39d695d065dc40e757b0099db
LIAISON Multi-Control Tumour Markers
TW: 禮雅尚多重腫瘤標記品管物質組
Registration details
- Analysis ID
- 363068c39d695d065dc40e757b0099db
- License Form
- Ministry of Health Medical Device Import No. 030512
- Customs Code
- DHA05603051201
Company information
- Manufacturer
- DIASORIN ITALIA S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- MEDRICH INSTRUMENT CO., LTD.
Product details
- Intended Use
- This product is designed to provide reliability in the analysis of tumor markers (AFP, CA 125 II, CA 15-3, CA 19-9, CEA, Ferritin, HCG and β2-Microglobulin) in serum by LIAISON and LIAISON XL automated immunofluorescence analyzers.
- 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
- Feb 27, 2018
- Expiry Date
- Feb 27, 2028
About this record
Access comprehensive regulatory information for LIAISON Multi-Control Tumour Markers in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 363068c39d695d065dc40e757b0099db and manufactured by DIASORIN ITALIA S.P.A.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
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