Taiwan FDA registration c58bc2fb5598dc8d21f72198c3885f43
"Alere" Influenza A & B (Non-sterile)
TW: "美艾利爾" A+B型流行性感冒病毒檢驗試驗組 (未滅菌)
Taiwan·Risk Class 1·MD·ALERE SCARBOROUGH, INC.·Registered May 29, 2015 – May 29, 2020CancelledRegistration details
- Analysis ID
- c58bc2fb5598dc8d21f72198c3885f43
- License Form
- Ministry of Health Medical Device Import No. 015280
- Customs Code
- DHA09401528000
Company information
- Manufacturer
- ALERE SCARBOROUGH, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Ariel Health Inc
Product details
- 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
- May 29, 2015
- Expiry Date
- May 29, 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" Influenza A & B (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 c58bc2fb5598dc8d21f72198c3885f43 and manufactured by ALERE SCARBOROUGH, INC.. The authorized representative in Taiwan is Ariel Health Inc.
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