"Siloam" Mycoplasma Pneumoniae Rapid Test (Non-Sterile) - Taiwan Registration b135ded9c542529531a468c62503fdb0
Access comprehensive regulatory information for "Siloam" Mycoplasma Pneumoniae Rapid Test (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 b135ded9c542529531a468c62503fdb0 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is Siloam Biotech Co., Ltd..
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Device Details
Registration Details
b135ded9c542529531a468c62503fdb0
Ministry of Health Medical Device Import No. 017878
DHA09401787805
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
Imported from abroad
Dates and Status
May 23, 2017
May 23, 2022