LIAISON XL HCG - Taiwan Registration d225c7720092edce7c8dd3b4f509067c
Access comprehensive regulatory information for LIAISON XL HCG in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d225c7720092edce7c8dd3b4f509067c and manufactured by DIASORIN ITALIA S.P.A.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
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Device Details
Registration Details
d225c7720092edce7c8dd3b4f509067c
Ministry of Health Medical Device Import No. 030488
DHA05603048801
Product Details
This product is used for the quantitative detection of human chorionic gonadotropins (hCG and รhCG) in serum in vitro. This test must be performed on the LIAISON analyzer series.
A Clinical chemistry and clinical toxicology
A1155 Human chorionic gonadotropin test system
Imported from abroad
Dates and Status
Jan 23, 2018
Jan 23, 2028