BECKMAN COULTER IGF-I IRMA Kit - Taiwan Registration e5f8c155ed6eca7cc24146dfd2d8413a
Access comprehensive regulatory information for BECKMAN COULTER IGF-I IRMA Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e5f8c155ed6eca7cc24146dfd2d8413a 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
Registration Details
e5f8c155ed6eca7cc24146dfd2d8413a
Ministry of Health Medical Device Import No. 028432
DHAS5602843203
Product Details
In vitro quantification of insulin growth factor type 1 in human serum and plasma using radioimmunoassay.
A Clinical chemistry and clinical toxicology
A1370 Human Growth Hormone Test System
Imported from abroad; Consent must be attached to the input (each input must be supported by the consent of the Atomic Energy Commission)
Dates and Status
May 26, 2016
May 26, 2026

