Taiwan FDA registration 7edb3b4ec80878e7a5a3463a814f4b57
Trinity TREP-SURE Anti-Treponema EIA
TW: 萃尼諦專一性抗梅毒螺旋體酵素免疫檢測系統
Taiwan·Risk Class 2·MD·TRINITY BIOTECH USA·Registered Apr 03, 2014 – Apr 03, 2019CancelledRegistration details
- Analysis ID
- 7edb3b4ec80878e7a5a3463a814f4b57
- License Form
- Ministry of Health Medical Device Import No. 025933
- Customs Code
- DHA05602593302
Company information
- Manufacturer
- TRINITY BIOTECH USA
- Manufacturer Country
- United States
- Authorized Representative
- TRUGENE DIAGNOSTICS, INC.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3820 Treponemal pallidum non-treponemal reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 03, 2014
- Expiry Date
- Apr 03, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for Trinity TREP-SURE Anti-Treponema EIA in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7edb3b4ec80878e7a5a3463a814f4b57 and manufactured by TRINITY BIOTECH USA. The authorized representative in Taiwan is TRUGENE DIAGNOSTICS, INC..
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