Taiwan FDA registration b92209c12e74f81a19f90d66fbf48ffd
"AnyCare" Influenza A/B Rapid Test (Non-Sterile)
TW: "關心您" A/B型流感快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·Asia Genomics Technology Co., Ltd. Factory 1·Registered Feb 12, 2018 – Feb 12, 2023ExpiredRegistration details
- Analysis ID
- b92209c12e74f81a19f90d66fbf48ffd
- License Form
- Ministry of Health Medical Device Manufacturing No. 007118
Company information
- Manufacturer
- Asia Genomics Technology Co., Ltd. Factory 1
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Asia Genomics Technology Co., Ltd. Factory 1
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
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 12, 2018
- Expiry Date
- Feb 12, 2023
About this record
Access comprehensive regulatory information for "AnyCare" Influenza 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 b92209c12e74f81a19f90d66fbf48ffd and manufactured by Asia Genomics Technology Co., Ltd. Factory 1. The authorized representative in Taiwan is Asia Genomics Technology Co., Ltd. Factory 1.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices