"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.
Device Details
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 ๅผๅธ้่ๅ็ดฐ่็ ๆฏ่กๆธ ่ฉฆๅ;; C.3020 ่ บ็ ๆฏ่กๆธ ่ฉฆๅ;; C.2900 ๅพฎ็็ฉๆจฃๆฌๆถ้ๅ่ผธ้ๅจๆ
Input;; Chinese goods
Dates and Status
Feb 03, 2021
Feb 03, 2026

