Taiwan FDA registration 7cc4a44b48d54f966456decabe4a79b3
Bondis Mini Naff Human Immunoglobulin G4 Set
TW: 邦迪斯迷你那夫人類免疫球蛋白 G4 套組
Registration details
- Analysis ID
- 7cc4a44b48d54f966456decabe4a79b3
- Customs Code
- DHA00601902909
Company information
- Manufacturer
- THE BINDING SITE GROUP LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Intended Use
- The reagent set provides in vitro detection of immunoglobulin IgG subtype: IgG4 in human serum, which can assist in the clinical diagnosis of abnormal metabolism of IgG4 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 Bondis Mini Naff Human Immunoglobulin G4 Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7cc4a44b48d54f966456decabe4a79b3 and manufactured by THE BINDING SITE GROUP LIMITED. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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