Taiwan FDA registration 92ac27e6f1d0d15d77273d385eff14cb
"Abbott" Dengue Dengue Immunoglobulin M Test Reagent
TW: "亞培"百而靈登革熱免疫球蛋白M檢驗試劑
Taiwan·Risk Class 2·ABBOTT DIAGNOSTICS KOREA INC.·Registered Dec 10, 2014 – Dec 10, 2029ActiveRegistration details
- Analysis ID
- 92ac27e6f1d0d15d77273d385eff14cb
- Customs Code
- DHA05602681208
Company information
- Manufacturer
- ABBOTT DIAGNOSTICS KOREA INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Abbott Rapid Diagnostics Health Corp.
Product details
- Intended Use
- Enzyme immunosorbent assay was used to qualitatively detect IgM antibodies to dengue virus in human serum.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.0002 登革熱病毒血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Dec 10, 2014
- Expiry Date
- Dec 10, 2029
About this record
Access comprehensive regulatory information for "Abbott" Dengue Dengue Immunoglobulin M Test Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 92ac27e6f1d0d15d77273d385eff14cb and manufactured by ABBOTT DIAGNOSTICS KOREA INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
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