Taiwan FDA registration 3338eb1a23c8d74c5b4db1dcf2a8b162

Reyde blood glucose testing system

TW: 瑞易德血糖測試系統
Taiwan flagTaiwan·Risk Class 2·Aksotek Company·Registered Apr 14, 2021 – Apr 14, 2026Expired
Registration details
Analysis ID
3338eb1a23c8d74c5b4db1dcf2a8b162
Company information
Manufacturer
Aksotek Company
Manufacturer Country
Taiwan, Province of China
Authorized Representative
Aksotek Company
Product details
Intended Use
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.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1345 Glucose Test System
Import Information
QMS/QSD;; 國產
Dates and status
Registration Date
Apr 14, 2021
Expiry Date
Apr 14, 2026
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About this record

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 3338eb1a23c8d74c5b4db1dcf2a8b162 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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