Taiwan FDA registration 544c4ca8f1bee73db9a4280c004b7f5d
"Response Biomedical" Flu A/B Rapid Test (Non-sterile)
TW: "瑞邦生醫" A/B型流行性感冒病毒快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·RESPONSE BIOMEDICAL CORPORATION·Registered Jan 05, 2016 – Jan 05, 2021ExpiredRegistration details
- Analysis ID
- 544c4ca8f1bee73db9a4280c004b7f5d
- License Form
- Ministry of Health Medical Device Import No. 016043
- Customs Code
- DHA09401604301
Company information
- Manufacturer
- RESPONSE BIOMEDICAL CORPORATION
- Manufacturer Country
- Canada
- Authorized Representative
- RECHI 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 devices
- Product Type (Level 2)
- C3330 Influenza virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 05, 2016
- Expiry Date
- Jan 05, 2021
About this record
Access comprehensive regulatory information for "Response Biomedical" Flu A/B Rapid Test (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 544c4ca8f1bee73db9a4280c004b7f5d and manufactured by RESPONSE BIOMEDICAL CORPORATION. The authorized representative in Taiwan is RECHI CO., LTD..
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