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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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fb1342faa8e526fd0c2627848cb58b64
Registration Details
Taiwan FDA Registration: fb1342faa8e526fd0c2627848cb58b64
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Device Details

MAINE FA Pneumonia/Pneumoniaplus Control (Non-sterile)
TW: ้บฅๅฐผ่‚บ็‚Žๅ“็ฎก่ฉฆๅŠ‘ๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

fb1342faa8e526fd0c2627848cb58b64

Ministry of Health Medical Device Import No. 021275

DHA09402127503

Company Information

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