Taiwan FDA registration 12e06a8f93f0f2257afdaa1477458552

"Jieko" adenovirus and respiratory fusion cell virus rapid test reagent (unsterilized)

TW: “傑試可” 腺病毒及呼吸道融合細胞病毒快速檢驗試劑(未滅菌)

Taiwan·Risk Class 1·HANGZHOU ALLTEST BIOTECH CO., LTD.·Registered Feb 03, 2021 – Feb 03, 2026Expired

Registration details

Analysis ID: 12e06a8f93f0f2257afdaa1477458552
Customs Code: DHA09600443607

Company information

Manufacturer: HANGZHOU ALLTEST BIOTECH CO., LTD.
Manufacturer Country: China
Authorized Representative: Chuang An Biomedical Co., Ltd.

Product details

Intended Use: 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.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3480 呼吸道融合細胞病毒血清試劑;; C.3020 腺病毒血清試劑;; C.2900 微生物樣本收集及輸送器材
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Feb 03, 2021
Expiry Date: Feb 03, 2026

About this record

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..

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