Taiwan FDA registration 0673dfb20e3c518e22ad89c4f60a34e8
HighQ Check Special Blood Glucose Monitoring System
TW: 長青血糖監測系統
Taiwan·Risk Class 2·MD·AEON DIAGNOSTIC TECHNOLOGY CORPORATION·Registered Nov 06, 2018 – Nov 06, 2023ExpiredRegistration details
- Analysis ID
- 0673dfb20e3c518e22ad89c4f60a34e8
- License Form
- Ministry of Health Medical Device Manufacturing No. 006259
Company information
- Manufacturer
- AEON DIAGNOSTIC TECHNOLOGY CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- AEON DIAGNOSTIC TECHNOLOGY CORPORATION
Product details
- Intended Use
- This product is only for in vitro testing, which can quantitatively detect the blood glucose value of fingertip microvascular whole blood, and is not suitable for neonatal testing.
- 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 06, 2018
- Expiry Date
- Nov 06, 2023
About this record
Access comprehensive regulatory information for HighQ Check Special 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 0673dfb20e3c518e22ad89c4f60a34e8 and manufactured by AEON DIAGNOSTIC TECHNOLOGY CORPORATION. The authorized representative in Taiwan is AEON DIAGNOSTIC TECHNOLOGY CORPORATION.
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