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The Binding Site Optilite Albumin Kit - Taiwan Registration 3ce5e71cad5e79e8363d26929446d3d2

Access comprehensive regulatory information for The Binding Site Optilite Albumin Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3ce5e71cad5e79e8363d26929446d3d2 and manufactured by THE BINDING SITE GROUP LTD. 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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3ce5e71cad5e79e8363d26929446d3d2
Registration Details
Taiwan FDA Registration: 3ce5e71cad5e79e8363d26929446d3d2
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Device Details

The Binding Site Optilite Albumin Kit
TW: ้‚ฆ่ฟชๆ–ฏๆญๆ™ฎ็พ…็™ฝ่›‹็™ฝๅˆ†ๆžๅฅ—็ต„
Risk Class 2
MD

Registration Details

3ce5e71cad5e79e8363d26929446d3d2

Ministry of Health Medical Device Import No. 032189

DHA05603218901

Company Information

United Kingdom

Product Details

This product is used with the Binding Site Plite analyzer for in vitro quantitative analysis of human serum and plasma albumin containing heparin lithium salts or EDTA anticoagulants.

A Clinical chemistry and clinical toxicology

A1035 Albumin Test System

Imported from abroad

Dates and Status

Feb 26, 2019

Feb 26, 2024