Taiwan FDA registration 6cd5a16c95f6899149247c1fadab5a2e
Omega leptospira rapid assay reagent
TW: 奧米加鉤端螺旋體快速檢驗試劑
Registration details
- Analysis ID
- 6cd5a16c95f6899149247c1fadab5a2e
- Customs Code
- DHA04400804707
Company information
- Manufacturer
- OMEGA DIAGNOSTICS LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EUGENE-CHEN CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the medical device management measures "Leptospira sera reagent (C.3350)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3350 鉤端螺旋菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Sep 07, 2009
- Expiry Date
- Sep 07, 2014
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Omega leptospira rapid assay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6cd5a16c95f6899149247c1fadab5a2e and manufactured by OMEGA DIAGNOSTICS LTD.. The authorized representative in Taiwan is EUGENE-CHEN CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices