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"IF" Rapid Helicobacter Test (non-sterile) - Taiwan Registration a86b3d98631e94851afa54bce3f18d82

Access comprehensive regulatory information for "IF" Rapid Helicobacter 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 a86b3d98631e94851afa54bce3f18d82 and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..

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a86b3d98631e94851afa54bce3f18d82
Registration Details
Taiwan FDA Registration: a86b3d98631e94851afa54bce3f18d82
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Device Details

"IF" Rapid Helicobacter Test (non-sterile)
TW: "็‘ฉ่Šณ"ๅนฝ้–€ๆ›ฒ็‹€ๆกฟ่Œๅฐฟ็ด ้…ถๅฟซ้€Ÿๆธฌ่ฉฆ็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a86b3d98631e94851afa54bce3f18d82

Ministry of Health Medical Device Manufacturing No. 007818

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".

C Immunology and microbiology devices

C0003 Helicobacter serological reagent

Produced in Taiwan, China

Dates and Status

Jun 24, 2019

Jun 24, 2024