Taiwan FDA registration b636c7c684e44f28f5a687def679f1b6
"Abbot" Platyling Dengue Antigen Test Tablets
TW: "亞培"百而靈登革熱NS1抗原測試片
Taiwan·Risk Class 2·ABBOTT DIAGNOSTICS KOREA INC.·Registered Sep 27, 2012 – Sep 27, 2027ActiveRegistration details
- Analysis ID
- b636c7c684e44f28f5a687def679f1b6
- Customs Code
- DHA00602408401
Company information
- Manufacturer
- ABBOTT DIAGNOSTICS KOREA INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Abbott Rapid Diagnostics Health Corp.
Product details
- Intended Use
- The Speedi Platin Dengue Antigen Test Tablet is a single-step qualitative determination of dengue virus NS1 antigen in human serum, plasma and whole blood by in vitro immunochromolayer analysis.
- 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
- Sep 27, 2012
- Expiry Date
- Sep 27, 2027
About this record
Access comprehensive regulatory information for "Abbot" Platyling Dengue Antigen Test Tablets in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b636c7c684e44f28f5a687def679f1b6 and manufactured by ABBOTT DIAGNOSTICS KOREA INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
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