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"AMA"RUT Pro (Non-Sterile) - Taiwan Registration faa4cd684f26968400d78ca5bd64a097

Access comprehensive regulatory information for "AMA"RUT Pro (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 faa4cd684f26968400d78ca5bd64a097 and manufactured by Association of Medicine and Analytics Company Limited. The authorized representative in Taiwan is JOLEX INTERNATIONAL 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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faa4cd684f26968400d78ca5bd64a097
Registration Details
Taiwan FDA Registration: faa4cd684f26968400d78ca5bd64a097
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Device Details

"AMA"RUT Pro (Non-Sterile)
TW: "ไบž้ฆฌ"ๅฐˆๆฅญๅž‹-ๅนฝ้–€่žบๆ—‹ๆกฟ่Œๅฐฟ็ด ้…ถๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

faa4cd684f26968400d78ca5bd64a097

Ministry of Health Medical Device Import No. 020465

DHA09402046503

Company Information

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

Imported from abroad

Dates and Status

May 21, 2019

May 21, 2024