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Reyde blood glucose testing system - Taiwan Registration 68d60c05d36731b2a09c1fe08354c162

Access comprehensive regulatory information for Reyde blood glucose testing system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 68d60c05d36731b2a09c1fe08354c162 and manufactured by Aksotek Company. The authorized representative in Taiwan is Aksotek Company.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Aksotek Company, and 1 recent registrations in the same category. 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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68d60c05d36731b2a09c1fe08354c162
Registration Details
Taiwan FDA Registration: 68d60c05d36731b2a09c1fe08354c162
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Device Details

Reyde blood glucose testing system
TW: ็‘žๆ˜“ๅพท่ก€็ณ–ๆธฌ่ฉฆ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

68d60c05d36731b2a09c1fe08354c162

DHY00500192806

Company Information

Taiwan, Province of China

Product Details

It is suitable for in vitro diagnostic use, as a monitoring of blood sugar, it can provide diabetic patients to self-detect fingertip microvascular blood glucose value, or provide professionals to detect venous or arterial whole blood and neonatal microvascular blood glucose value.

A Clinical chemistry and clinical toxicology

A.1345 Glucose Test System

Domestic

Dates and Status

Nov 18, 2005

Nov 18, 2020

May 05, 2021

Cancellation Information

Logged out

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