Taiwan FDA registration 0a281b699a26412ffcc9c9c675b4a7c1
Peace Syphilis serum test reagent
TW: 和平梅毒血清試驗試劑
Registration details
- Analysis ID
- 0a281b699a26412ffcc9c9c675b4a7c1
- Customs Code
- DHA00601583401
Company information
- Manufacturer
- TECO DIAGNOSTICS
- Manufacturer Country
- United States
- Authorized Representative
- HO-PING INSTRUMENT CO., LTD.
Product details
- Intended Use
- Rapid plasma reagin (RPR) is a non-helical flocculation test, qualitative and semi-quantitative human serum or plasma reagin antibodies.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3820 Treponema pallidum non-spirochal test
- Import Information
- import
Dates and status
- Registration Date
- Jan 05, 2006
- Expiry Date
- Jan 05, 2011
- Cancellation Date
- Dec 29, 2011
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Peace Syphilis serum test reagent in Taiwan's medical device market through Pure Global AI's free database. is registered under number 0a281b699a26412ffcc9c9c675b4a7c1 and manufactured by TECO DIAGNOSTICS. The authorized representative in Taiwan is HO-PING INSTRUMENT CO., LTD..
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