Taiwan FDA registration ad68f9acc2517db402cdc4269b3af00a
Novartis ketone test system (unsterilized)
TW: "諾華" 酮體測試系統 (未滅菌)
Registration details
- Analysis ID
- ad68f9acc2517db402cdc4269b3af00a
- Customs Code
- DHA09402014501
Company information
- Manufacturer
- NOVA BIOMEDICAL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- BEAM INTERNATIONAL INC.
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
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 06, 2019
- Expiry Date
- Mar 06, 2029
About this record
Access comprehensive regulatory information for Novartis ketone test system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ad68f9acc2517db402cdc4269b3af00a and manufactured by NOVA BIOMEDICAL CORPORATION. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..
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