Taiwan FDA registration 30bff5a3cea5b71721c72d2e2e4205cc
Alere i Influenza A&B
TW: 美艾利爾流行性感冒病毒核酸檢驗試劑
Taiwan·Risk Class 2·MD·ALERE SCARBOROUGH, INC.·Registered Dec 16, 2015 – Dec 16, 2020CancelledRegistration details
- Analysis ID
- 30bff5a3cea5b71721c72d2e2e4205cc
- License Form
- Ministry of Health Medical Device Import No. 027999
- Customs Code
- DHA05602799903
Company information
- Manufacturer
- ALERE SCARBOROUGH, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Abbott Rapid Diagnostics Health Corp.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3980 Multi-standard nucleic acid test reagent for respiratory viruses
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 16, 2015
- Expiry Date
- Dec 16, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Alere i Influenza A&B in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 30bff5a3cea5b71721c72d2e2e4205cc and manufactured by ALERE SCARBOROUGH, INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
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.
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