Taiwan FDA registration 18fb1f968cef62ad10cba2d4cc3c2078

"Siloa" Rotavirus/Adenovirus 2-in-1 Test Set (Unsterilized)

TW: "西羅亞" 輪狀病毒/腺病毒二合一檢驗試劑組 (未滅菌)

Taiwan·Risk Class 1·HANGZHOU ALLTEST BIOTECH CO., LTD.·Registered Jan 28, 2021 – Jan 28, 2026Expired

Registration details

Analysis ID: 18fb1f968cef62ad10cba2d4cc3c2078
Customs Code: DHA09600440407

Company information

Manufacturer: HANGZHOU ALLTEST BIOTECH CO., LTD.
Manufacturer Country: China
Authorized Representative: Siloam Biotech Co., Ltd.

Product details

Intended Use: It is limited to the first-level identification scope of the "Adenovirus Serum Reagent (C.3020)" and "Poliovirus Serum Reagent (C.3405)" of the Classification and Grading Management Measures for Medical Devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3020 腺病毒血清試劑;; C.3405 小兒麻痺病毒血清試劑
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Jan 28, 2021
Expiry Date: Jan 28, 2026

About this record

Access comprehensive regulatory information for "Siloa" Rotavirus/Adenovirus 2-in-1 Test Set (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 18fb1f968cef62ad10cba2d4cc3c2078 and manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD.. The authorized representative in Taiwan is Siloam Biotech Co., Ltd..

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