Bondis Human Immunoglobulin G Subtype Test Kit - Taiwan Registration d4b4ddefdded47ed5c465ab05ef1e741
Access comprehensive regulatory information for Bondis Human Immunoglobulin G Subtype Test Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d4b4ddefdded47ed5c465ab05ef1e741 and manufactured by THE BINDING SITE GROUP LIMITED. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Product Details
This panel is intended for in vitro diagnostic use to quantify human serum immunoglobulin G subtypes. This kit is available for Hitachi 911/912/917/Hitachi Modular P instruments.
C Immunology and microbiology
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import
Dates and Status
Sep 30, 2010
Sep 30, 2020
May 19, 2022
Cancellation Information
Logged out
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