Taiwan FDA registration a14d6b776645d2db1650872a2219e23a
"SD" Bioline Influenza Ultra (Non-Sterile)
TW: "速帝" 百而靈流感病毒抗原快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·STANDARD DIAGNOSTICS, INC.·Registered Apr 22, 2015 – Jul 28, 2020CancelledRegistration details
- Analysis ID
- a14d6b776645d2db1650872a2219e23a
- License Form
- Ministry of Health Medical Device Import No. 015138
- Customs Code
- DHA09401513807
Company information
- Manufacturer
- STANDARD DIAGNOSTICS, INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Abbott Rapid Diagnostics Health Corp.
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
- Apr 22, 2015
- Expiry Date
- Jul 28, 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 "SD" Bioline Influenza Ultra (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 a14d6b776645d2db1650872a2219e23a and manufactured by STANDARD DIAGNOSTICS, INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
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