Taiwan FDA registration faa4cd684f26968400d78ca5bd64a097

"AMA"RUT Pro (Non-Sterile)

TW: "亞馬"專業型-幽門螺旋桿菌尿素酶檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·MD·Association of Medicine and Analytics Company Limited·Registered May 21, 2019 – May 21, 2024Expired

Registration details

Analysis ID: faa4cd684f26968400d78ca5bd64a097
License Form: Ministry of Health Medical Device Import No. 020465
Customs Code: DHA09402046503

Company information

Manufacturer: Association of Medicine and Analytics Company Limited
Manufacturer Country: Russian Federation
Authorized Representative: JOLEX INTERNATIONAL CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C0003 Helicobacter serological reagent
Import Information: Imported from abroad

Dates and status

Registration Date: May 21, 2019
Expiry Date: May 21, 2024

About this record

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..

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