Taiwan FDA registration 2bac9cf885d1366740626354d9ef514f
QuickVue Influenza A+B Test
TW: “速利”流行性感冒病毒A型和B型測定試劑
Taiwan·Risk Class 2·MD·QUIDEL CORPORATION·Registered Jul 17, 2020 – Jul 17, 2025ExpiredRegistration details
- Analysis ID
- 2bac9cf885d1366740626354d9ef514f
- License Form
- Ministry of Health Medical Device Import No. 033508
- Customs Code
- DHA05603350809
Company information
- Manufacturer
- QUIDEL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- BIO-CHECK LABORATORIES LTD.
Product details
- Intended Use
- This product is a rapid qualitative test of influenza virus type A and B antigens used in nasal swabs, nasopharyngeal swabs, nasal aspiration fluid and nasal irrigation fluid samples.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3328 Influenza Virus Antigen Rapid Screening System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 17, 2020
- Expiry Date
- Jul 17, 2025
About this record
Access comprehensive regulatory information for QuickVue Influenza A+B Test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2bac9cf885d1366740626354d9ef514f and manufactured by QUIDEL CORPORATION. The authorized representative in Taiwan is BIO-CHECK LABORATORIES LTD..
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