Pure Global

Luxcon blood glucose monitoring system - Taiwan Registration 215aff1f74cf01941709d6ed49a6c743

Access comprehensive regulatory information for Luxcon blood glucose monitoring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 215aff1f74cf01941709d6ed49a6c743 and manufactured by Hometech Biotechnology Co., Ltd.;; GLUCOPLUS INC.. The authorized representative in Taiwan is U-E CHECK MEDICAL 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
215aff1f74cf01941709d6ed49a6c743
Registration Details
Taiwan FDA Registration: 215aff1f74cf01941709d6ed49a6c743
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Luxcon blood glucose monitoring system
TW: ๆจ‚้ฉๅบท่ก€็ณ–็›ฃๆธฌ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

215aff1f74cf01941709d6ed49a6c743

DHY00500216001

Company Information

Canada;;Taiwan, Province of China

Product Details

Test the blood glucose concentration.

A Clinical chemistry and clinical toxicology

A.1345 Glucose Test System

Domestic

Dates and Status

Jun 06, 2006

Jun 06, 2021

Oct 12, 2023

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€