Taiwan FDA registration d68fe2a95199d4d683bc2ddc18412608

"IF"Mycoplasma Pneumoniae IgM rapid test cassette(non-sterile)

TW: "瑩芳"肺炎黴漿菌IgM快速檢測試劑盒(未滅菌)

Taiwan·Risk Class 1·MD·Yingfang Co., Ltd. Taichung Factory·Registered Dec 06, 2018 – Dec 06, 2023Expired

Registration details

Analysis ID: d68fe2a95199d4d683bc2ddc18412608
License Form: Ministry of Health Medical Device Manufacturing No. 007559

Company information

Manufacturer: Yingfang Co., Ltd. Taichung Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: IN FUNG 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: Produced in Taiwan, China

Dates and status

Registration Date: Dec 06, 2018
Expiry Date: Dec 06, 2023

About this record

Access comprehensive regulatory information for "IF"Mycoplasma Pneumoniae IgM rapid test cassette(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 d68fe2a95199d4d683bc2ddc18412608 and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..

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