Taiwan FDA registration a0ccd091083442311027c1d044b35775
The Binding Site Hevylite Human IgM Lambda Kit
TW: 邦迪斯倫達型人類免疫球蛋白M輕鏈分析套組
Taiwan·Risk Class 2·MD·THE BINDING SITE GROUP LTD·Registered May 25, 2018 – May 25, 2023ExpiredRegistration details
- Analysis ID
- a0ccd091083442311027c1d044b35775
- License Form
- Ministry of Health Medical Device Import No. 031125
- Customs Code
- DHA05603112509
Company information
- Manufacturer
- THE BINDING SITE GROUP LTD
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Intended Use
- This product is used with a SPAPLUS analyzer to quantify Lenda-type immunoglobulin M (IgM lambda) in human serum.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C5510 Immunoglobulins A, G, M, D and E Immunoassay System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 25, 2018
- Expiry Date
- May 25, 2023
About this record
Access comprehensive regulatory information for The Binding Site Hevylite Human IgM Lambda Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0ccd091083442311027c1d044b35775 and manufactured by THE BINDING SITE GROUP LTD. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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