Taiwan FDA registration b9e6bf488f0f0a57354e23c57250b647

Relmex blood glucose testing system

TW: 瑞爾美血糖測試系統
Taiwan flagTaiwan·Risk Class 2·Aksotek Company·Registered Dec 01, 2008 – Nov 18, 2020Cancelled
Registration details
Analysis ID
b9e6bf488f0f0a57354e23c57250b647
Customs Code
DHY00500271609
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
Domestic
Dates and status
Registration Date
Dec 01, 2008
Expiry Date
Nov 18, 2020
Cancellation Date
Apr 14, 2021
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for Relmex 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 b9e6bf488f0f0a57354e23c57250b647 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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