"Dynax" Enzyme Analyzer for Clinical Use (Unsterilized)
Taiwan·Risk Class 1·DYNEX TECHNOLOGIES INC.·Registered Sep 16, 2021 – Sep 16, 2026Cancelled- Analysis ID
- 13021cdb9924b78d5b004ddce57d3a9a
- Customs Code
- DHA09402265301
- Manufacturer
- DYNEX TECHNOLOGIES INC.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRI CO., LTD.
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Enzyme Analyzer for Clinical Use (A.2500)" first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2500 Enzyme analyzer for clinical use
- Import Information
- Input;; QMS/QSD
- Registration Date
- Sep 16, 2021
- Expiry Date
- Sep 16, 2026
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Dynax" Enzyme Analyzer for Clinical Use (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 13021cdb9924b78d5b004ddce57d3a9a and manufactured by DYNEX TECHNOLOGIES INC.. The authorized representative in Taiwan is MEDTRI CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DYNEX TECHNOLOGIES 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.