Taiwan FDA registration 966989b811aef6a8a13fc7929653eb7e
PIIP Rapid Detection Reagent for Influenza A/B Virus (Unsterilized)
TW: "博拓" A/B型流感病毒快速檢測試劑 (未滅菌)
Taiwan·Risk Class 1·HANGZHOU BIOTEST BIOTECH CO., LTD.·Registered Jul 26, 2017 – Jul 26, 2022CancelledRegistration details
- Analysis ID
- 966989b811aef6a8a13fc7929653eb7e
- Customs Code
- DHA09600315800
Company information
- Manufacturer
- HANGZHOU BIOTEST BIOTECH CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
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
- Chinese goods;; input
Dates and status
- Registration Date
- Jul 26, 2017
- Expiry Date
- Jul 26, 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 PIIP Rapid Detection Reagent for Influenza A/B Virus (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 966989b811aef6a8a13fc7929653eb7e and manufactured by HANGZHOU BIOTEST BIOTECH CO., LTD.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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