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"Tauns" Mycoplasma Pneumoniae Rapid Test (Non-Sterile) - Taiwan Registration 37d33659e52e02d61abcbdd498b2ee2c

Access comprehensive regulatory information for "Tauns" 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 37d33659e52e02d61abcbdd498b2ee2c and manufactured by TAUNS LABORATORIES, INC.. The authorized representative in Taiwan is YOULUM BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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37d33659e52e02d61abcbdd498b2ee2c
Registration Details
Taiwan FDA Registration: 37d33659e52e02d61abcbdd498b2ee2c
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Device Details

"Tauns" Mycoplasma Pneumoniae Rapid Test (Non-Sterile)
TW: "่—คๅธ" ่‚บ็‚Ž้ปดๆผฟ่Œๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

37d33659e52e02d61abcbdd498b2ee2c

Ministry of Health Medical Device Import No. 015979

DHA09401597901

Company Information

Japan

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

Dec 16, 2015

Dec 16, 2025