Beckman Coulter Human Chorionic Gonadotropin Radioimmunoassay Set - Taiwan Registration 78a74e3a49efb5bce7d633cc1a61d638
Access comprehensive regulatory information for Beckman Coulter Human Chorionic Gonadotropin Radioimmunoassay Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 78a74e3a49efb5bce7d633cc1a61d638 and manufactured by IMMUNOTECH S.R.O.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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Device Details
Product Details
In vitro quantification of total chorionic gonadotropin in human serum and plasma using radioimmunoassay.
A Clinical chemistry and clinical toxicology
A.1660 Grade Material (Analysis Material Non-Analysis);; A.1150 Calibrated Products;; A.1155 Human chorionic gonadal heterinology
Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and Status
Mar 04, 2016
Mar 04, 2026