Taiwan FDA registration 4d2b1dc69a44e571a722ae511ec40ec5
Bundis Human Immunoglobulin G Set
TW: 邦迪斯人類免疫球蛋白G套組
Taiwan·Risk Class 2·THE BINDING SITE GROUP LIMITED·Registered Oct 23, 2012 – Oct 23, 2027ActiveRegistration details
- Analysis ID
- 4d2b1dc69a44e571a722ae511ec40ec5
- Customs Code
- DHA00602410009
Company information
- Manufacturer
- THE BINDING SITE GROUP LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Intended Use
- Quantitative detection of immunoglobulin G (IgG) and immunoglobulin G subclasses (IgG subclasses 1, 2, 3, 4) in human serum must be used with a SPAPLUS analyzer.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5510 免疫球蛋白A,G,M,D及E免疫試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Oct 23, 2012
- Expiry Date
- Oct 23, 2027
About this record
Access comprehensive regulatory information for Bundis Human Immunoglobulin G Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4d2b1dc69a44e571a722ae511ec40ec5 and manufactured by THE BINDING SITE GROUP LIMITED. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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