Taiwan FDA registration 9e5f70e1a0da78bb8b4a4828e3fdbef7
SD BIOLINE Dengue IgG/IgM WB
TW: 速帝百而靈登革熱IgG/IgM抗體快速測試片
Taiwan·Risk Class 2·MD·STANDARD DIAGNOSTICS, INC.·Registered Apr 07, 2015 – Apr 07, 2020CancelledRegistration details
- Analysis ID
- 9e5f70e1a0da78bb8b4a4828e3fdbef7
- License Form
- Ministry of Health Medical Device Import No. 027199
- Customs Code
- DHA05602719900
Company information
- Manufacturer
- STANDARD DIAGNOSTICS, INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Ariel Health Inc
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C0002 Dengue virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 07, 2015
- Expiry Date
- Apr 07, 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 Dengue IgG/IgM WB in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e5f70e1a0da78bb8b4a4828e3fdbef7 and manufactured by STANDARD DIAGNOSTICS, INC.. The authorized representative in Taiwan is Ariel Health Inc.
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