Taiwan FDA registration 3a693793bb3f68f8e4626ee97165daff
Ashbo blood glucose ketone test system
TW: 艾士博血糖血酮測試系統
Taiwan·Risk Class 2·Taibo Technology Co., Ltd. five-stock factory·Registered Mar 14, 2022 – Mar 14, 2027ActiveRegistration details
- Analysis ID
- 3a693793bb3f68f8e4626ee97165daff
Company information
- Manufacturer
- Taibo Technology Co., Ltd. five-stock factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIDOC TECHNOLOGY CORPORATION
Product details
- Intended Use
- This product is an in vitro diagnostic medical device that can quantitatively detect the concentration of glucose and ketone bodies in fresh fingertip whole blood and venous whole blood, and is intended for professional use only.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1435 Ketone (non-quantitative) testing system;; A.1345 Glucose Test System
- Import Information
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Mar 14, 2022
- Expiry Date
- Mar 14, 2027
About this record
Access comprehensive regulatory information for Ashbo blood glucose ketone test system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3a693793bb3f68f8e4626ee97165daff and manufactured by Taibo Technology Co., Ltd. five-stock factory. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.
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