"Innova" Bayer Flexun Automatic Enzyme Immunity Analyzer (Unsterilized)
Taiwan·Risk Class 1·INOVA DIAGNOSTICS, INC.·Registered Aug 07, 2019 – Aug 07, 2024Cancelled- Analysis ID
- db8e7a2d1facba05f72bafbf1bdafebf
- Customs Code
- DHA09402073901
- Manufacturer
- INOVA DIAGNOSTICS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- TRUGENE DIAGNOSTICS, INC.
- Intended Use
- Limited to the first level identification range of enzyme analyzer for clinical use (A.2500) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2500 Enzyme analyzer for clinical use
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Aug 07, 2019
- Expiry Date
- Aug 07, 2024
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Innova" Bayer Flexun Automatic Enzyme Immunity Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number db8e7a2d1facba05f72bafbf1bdafebf and manufactured by INOVA DIAGNOSTICS, INC.. The authorized representative in Taiwan is TRUGENE DIAGNOSTICS, INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including INOVA DIAGNOSTICS, INC., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.