Taiwan FDA registration 74b982a7d3e5031cbc71e69fbee4550d
Bundis Mini Naff Human Immunoglobulin G3 Set
TW: 邦迪斯迷你那夫人類免疫球蛋白 G3 套組
Registration details
- Analysis ID
- 74b982a7d3e5031cbc71e69fbee4550d
- Customs Code
- DHA00601902807
Company information
- Manufacturer
- THE BINDING SITE GROUP LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Intended Use
- The kit provides in vitro detection of immunoglobulin IgG subtype: IgG3 in human serum, which can assist in the clinical diagnosis of abnormal metabolism of IgG3 in the human body, and the set is suitable for MININEPH TM turbidity meter as an experimental operation platform.
- 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
- May 07, 2008
- Expiry Date
- May 07, 2023
About this record
Access comprehensive regulatory information for Bundis Mini Naff Human Immunoglobulin G3 Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 74b982a7d3e5031cbc71e69fbee4550d and manufactured by THE BINDING SITE GROUP LIMITED. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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