Taiwan FDA registration bb3cfaf4ad3074e258e0526b2e569dfa
Kono mini blood glucose monitoring system
TW: 可諾 迷你血糖監測系統
Registration details
- Analysis ID
- bb3cfaf4ad3074e258e0526b2e569dfa
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- KERNEL INT'L CORP.
Product details
- Intended Use
- This product is for quantitative detection of blood glucose content in fingertip microvascular whole blood, which can be used for personal self-testing, and is not suitable for newborn testing.
- Product Type (Level 1)
- A Clinical Chemistry and Clinical Toxicology;; I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Manual instruments for general surgery; A.1345 Glucose Test System
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Jan 12, 2017
- Expiry Date
- Jan 12, 2022
- Cancellation Date
- Aug 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Kono mini 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 bb3cfaf4ad3074e258e0526b2e569dfa and manufactured by Nine Feather International Enterprises Limited;; Yuxin Biotechnology Co., Ltd. The authorized representative in Taiwan is KERNEL INT'L CORP..
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