MAINE FA Pneumonia/Pneumoniaplus Control (Non-sterile) - Taiwan Registration fb1342faa8e526fd0c2627848cb58b64
Access comprehensive regulatory information for MAINE FA Pneumonia/Pneumoniaplus Control (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 fb1342faa8e526fd0c2627848cb58b64 and manufactured by Maine Molecular Quality Controls, Inc.. The authorized representative in Taiwan is DITECH ENTERPRISE CO., LTD..
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Device Details
Registration Details
fb1342faa8e526fd0c2627848cb58b64
Ministry of Health Medical Device Import No. 021275
DHA09402127503
Product Details
Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
A Clinical chemistry and clinical toxicology
A1660 Quality Control Materials (Analytical and Non-Analytical)
Imported from abroad
Dates and Status
Feb 17, 2020
Feb 17, 2025

