Taiwan FDA registration 37d33659e52e02d61abcbdd498b2ee2c

"Tauns" Mycoplasma Pneumoniae Rapid Test (Non-Sterile)

TW: "藤司" 肺炎黴漿菌檢測試劑 (未滅菌)

Taiwan·Risk Class 1·MD·TAUNS LABORATORIES, INC.·Registered Dec 16, 2015 – Dec 16, 2025Expired

Registration details

Analysis ID: 37d33659e52e02d61abcbdd498b2ee2c
License Form: Ministry of Health Medical Device Import No. 015979
Customs Code: DHA09401597901

Company information

Manufacturer: TAUNS LABORATORIES, INC.
Manufacturer Country: Japan
Authorized Representative: YOULUM BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Mycoplasma Serological Reagent (C.3375)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C3375 Mycoplasma serum reagent
Import Information: Imported from abroad

Dates and status

Registration Date: Dec 16, 2015
Expiry Date: Dec 16, 2025

About this record

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..

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