Taiwan FDA registration aa1e5373bedb949dbaf1ca1427f44592
Omega Syphilis Non-Helical Rapid Lectin Reagent
TW: 奧米加梅毒非螺旋快速凝集素試劑
Taiwan·Risk Class 2·OMEGA DIAGNOSTICS LTD.·Registered Mar 13, 2006 – Mar 13, 2021CancelledRegistration details
- Analysis ID
- aa1e5373bedb949dbaf1ca1427f44592
- Customs Code
- DHA00601612401
Company information
- Manufacturer
- OMEGA DIAGNOSTICS LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EUGENE-CHEN CO., LTD.
Product details
- Intended Use
- A non-spirochetal agglutination reagent panel for the detection of syphilis reagin antibodies in serum and plasma.
- 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
- Mar 13, 2006
- Expiry Date
- Mar 13, 2021
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Omega Syphilis Non-Helical Rapid Lectin Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa1e5373bedb949dbaf1ca1427f44592 and manufactured by OMEGA DIAGNOSTICS LTD.. The authorized representative in Taiwan is EUGENE-CHEN CO., LTD..
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