"IF"Mycoplasma Pneumoniae IgM rapid test cassette(non-sterile) - Taiwan Registration d68fe2a95199d4d683bc2ddc18412608
Access comprehensive regulatory information for "IF"Mycoplasma Pneumoniae IgM rapid test cassette(non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d68fe2a95199d4d683bc2ddc18412608 and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..
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Device Details
Registration Details
d68fe2a95199d4d683bc2ddc18412608
Ministry of Health Medical Device Manufacturing No. 007559
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Mycoplasma Serological Reagent (C.3375)".
C Immunology and microbiology devices
C3375 Mycoplasma serum reagent
Produced in Taiwan, China
Dates and Status
Dec 06, 2018
Dec 06, 2023