Taiwan FDA registration 1640adc32124697d576abf45b1659b85
"Siloa" Influenza Virus A&B Rapid Test Reagent (Unsterilized)
TW: "西羅亞" 流感病毒A&B快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·WUHAN JIN PU MAN BIOTECH CO., LTD·Registered May 23, 2017 – May 23, 2022CancelledRegistration details
- Analysis ID
- 1640adc32124697d576abf45b1659b85
- Customs Code
- DHA09600308907
Company information
- Manufacturer
- WUHAN JIN PU MAN BIOTECH CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- Siloam Biotech Co., Ltd.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3330 流感病毒血清試劑
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- May 23, 2017
- Expiry Date
- May 23, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Siloa" Influenza Virus A&B 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 1640adc32124697d576abf45b1659b85 and manufactured by WUHAN JIN PU MAN BIOTECH CO., LTD. The authorized representative in Taiwan is Siloam Biotech Co., Ltd..
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