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
Taiwan flagTaiwan·Risk Class 2·THE BINDING SITE GROUP LIMITED·Registered May 07, 2008 – May 07, 2023Expired
Registration details
Analysis ID
7cc4a44b48d54f966456decabe4a79b3
Customs Code
DHA00601902909
Company information
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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