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"Jieko" adenovirus and respiratory fusion cell virus rapid test reagent (unsterilized) - Taiwan Registration 12e06a8f93f0f2257afdaa1477458552

Access comprehensive regulatory information for "Jieko" adenovirus and respiratory fusion cell virus rapid test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 12e06a8f93f0f2257afdaa1477458552 and manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD.. The authorized representative in Taiwan is Chuang An Biomedical 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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12e06a8f93f0f2257afdaa1477458552
Registration Details
Taiwan FDA Registration: 12e06a8f93f0f2257afdaa1477458552
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Device Details

"Jieko" adenovirus and respiratory fusion cell virus rapid test reagent (unsterilized)
TW: โ€œๅ‚‘่ฉฆๅฏโ€ ่…บ็—…ๆฏ’ๅŠๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’ๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

12e06a8f93f0f2257afdaa1477458552

DHA09600443607

Company Information

Product Details

It is limited to the first level of identification of "adenovirus serum reagent (C.3020)", "microbial sample collection and delivery equipment (C.2900)" and "respiratory fusion cell virus serum reagent (C.3480)" of the classification and grading management measures for medical devices.

C Immunology and microbiology

C.3480 ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘;; C.3020 ่…บ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘;; C.2900 ๅพฎ็”Ÿ็‰ฉๆจฃๆœฌๆ”ถ้›†ๅŠ่ผธ้€ๅ™จๆ

Input;; Chinese goods

Dates and Status

Feb 03, 2021

Feb 03, 2026