Taiwan FDA registration 0387be59c3c52c327489ffc512e08088
HMD Go Easy Blood Glucose Monitoring System
TW: 厚美德金輕鬆血糖檢測系統
Taiwan·Risk Class 2·MD·HMD BIOMEDICAL INC.·Registered Nov 23, 2018 – Jun 20, 2026ExpiredRegistration details
- Analysis ID
- 0387be59c3c52c327489ffc512e08088
- License Form
- Ministry of Health Medical Device Manufacturing No. 006265
Company information
- Manufacturer
- HMD BIOMEDICAL INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HMD BIOMEDICAL INC.
Product details
- Intended Use
- This product is made using electrochemical biosensing technology and can only be used with Houmei Dejin Ecliba blood glucose test tablets to provide diabetic patients with home detection of microvascular whole blood glucose values. And under the operation of professionals, the blood glucose value of adult microvascular, venous blood and whole blood of newborn infants can be measured.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1345 Glucose Test System
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 23, 2018
- Expiry Date
- Jun 20, 2026
About this record
Access comprehensive regulatory information for HMD Go Easy 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 0387be59c3c52c327489ffc512e08088 and manufactured by HMD BIOMEDICAL INC.. The authorized representative in Taiwan is HMD BIOMEDICAL INC..
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 DatabasePowered by Pure Global AI89,000+ Devices