Taiwan FDA registration 215aff1f74cf01941709d6ed49a6c743
Luxcon blood glucose monitoring system
TW: 樂適康血糖監測系統
Taiwan·Risk Class 2·Hometech Biotechnology Co., Ltd.;; GLUCOPLUS INC.·Registered Jun 06, 2006 – Jun 06, 2021CancelledRegistration details
- Analysis ID
- 215aff1f74cf01941709d6ed49a6c743
- Customs Code
- DHY00500216001
Company information
- Manufacturer Country
- Canada;;Taiwan, Province of China
- Authorized Representative
- U-E CHECK MEDICAL CO., LTD.
Product details
- Intended Use
- Test the blood glucose concentration.
- 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
- Jun 06, 2006
- Expiry Date
- Jun 06, 2021
- Cancellation Date
- Oct 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Luxcon 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 215aff1f74cf01941709d6ed49a6c743 and manufactured by Hometech Biotechnology Co., Ltd.;; GLUCOPLUS INC.. The authorized representative in Taiwan is U-E CHECK MEDICAL CO., LTD..
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