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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.

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Registration Details
Taiwan FDA Registration: d4b4ddefdded47ed5c465ab05ef1e741
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Device Details

Bondis Human Immunoglobulin G Subtype Test Kit
TW: ้‚ฆ่ฟชๆ–ฏไบบ้กžๅ…็–ซ็ƒ่›‹็™ฝGไบžๅž‹ๆชข้ฉ—่ฉฆๅŠ‘ๅฅ—็ต„
Risk Class 2
Cancelled

Registration Details

d4b4ddefdded47ed5c465ab05ef1e741

DHA00602155305

Company Information

United Kingdom

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

C.5510 ๅ…็–ซ็ƒ่›‹็™ฝA,G,M,DๅŠEๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Sep 30, 2010

Sep 30, 2020

May 19, 2022

Cancellation Information

Logged out

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