Taiwan FDA registration e4e13c1e8047fa5f0b683d011aef07c0
Rhett Gee-ketone Test Tablets (Unsterilized)
TW: 瑞特 吉易酮體測試片 (未滅菌)
Taiwan·Risk Class 1·Daqing Factory of Huaguang Biotechnology Co., Ltd·Registered Sep 21, 2022 – Sep 21, 2027ActiveRegistration details
- Analysis ID
- e4e13c1e8047fa5f0b683d011aef07c0
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Daqing Factory of Huaguang Biotechnology Co., Ltd
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment "Ketone (non-quantitative) test system (A.1435)" first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1435 Ketone (non-quantitative) testing system
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Sep 21, 2022
- Expiry Date
- Sep 21, 2027
About this record
Access comprehensive regulatory information for Rhett Gee-ketone Test Tablets (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e4e13c1e8047fa5f0b683d011aef07c0 and manufactured by Daqing Factory of Huaguang Biotechnology Co., Ltd. The authorized representative in Taiwan is Daqing Factory of Huaguang Biotechnology Co., Ltd.
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