Taiwan FDA registration be418389a9f27e67daff14919c6cdac2
Treponema pallidum hemoagglutination reagent
TW: 奧米加梅毒螺旋體血球凝集試劑
Taiwan·Risk Class 2·OMEGA DIAGNOSTICS LTD.·Registered Mar 15, 2006 – Mar 15, 2021CancelledRegistration details
- Analysis ID
- be418389a9f27e67daff14919c6cdac2
- Customs Code
- DHA00601615907
Company information
- Manufacturer
- OMEGA DIAGNOSTICS LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EUGENE-CHEN CO., LTD.
Product details
- Intended Use
- 被動血球凝集法測試人體血清或腦脊髓液中的梅毒螺旋體(Treponema pallidum)抗體.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3830 Treponema pallidum test
- Import Information
- import
Dates and status
- Registration Date
- Mar 15, 2006
- Expiry Date
- Mar 15, 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 Treponema pallidum hemoagglutination reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be418389a9f27e67daff14919c6cdac2 and manufactured by OMEGA DIAGNOSTICS LTD.. The authorized representative in Taiwan is EUGENE-CHEN CO., LTD..
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