LANNER Immunoglobulin E Reagent Kit/IgE - Taiwan Registration a36c0bfb642fcdcd01f19ab5c3680e31
Access comprehensive regulatory information for LANNER Immunoglobulin E Reagent Kit/IgE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a36c0bfb642fcdcd01f19ab5c3680e31 and manufactured by LANNER BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LANNER BIOTECHNOLOGY CO., LTD..
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Device Details
Registration Details
a36c0bfb642fcdcd01f19ab5c3680e31
Ministry of Health Medical Device Manufacturing No. 005988
Product Details
It is used for in vitro quantitative analysis of immunoglobulin E content in human serum or EDTA and heparin plasma, suitable for Hitachi 7170 automatic biochemistry analyzer.
C Immunology and microbiology devices
C5510 Immunoglobulins A, G, M, D and E Immunoassay System
Produced in Taiwan, China
Dates and Status
Jul 17, 2018
Jul 17, 2028