Taiwan FDA registration 041428529bf197038a65c55a3c6e01b5
Lundor rapid plasma reagin reagent
TW: 倫多快速血漿反應素試劑
Taiwan·RANDOX LABORATORIES LTD·Registered Dec 12, 2005 – Dec 12, 2010CancelledRegistration details
- Analysis ID
- 041428529bf197038a65c55a3c6e01b5
- Customs Code
- DHA00601546802
Company information
- Manufacturer
- RANDOX LABORATORIES LTD
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EUGENE-CHEN CO., LTD.
Product details
- Intended Use
- Quantification of plum pigments 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
- Dec 12, 2005
- Expiry Date
- Dec 12, 2010
- Cancellation Date
- Oct 29, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Lundor rapid plasma reagin reagent in Taiwan's medical device market through Pure Global AI's free database. is registered under number 041428529bf197038a65c55a3c6e01b5 and manufactured by RANDOX LABORATORIES 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