"Dynex" Disco Clinical Use Enzyme Analyzer (Unsterilized)
Taiwan·Risk Class 1·DYNEX TECHNOLOGIES INC.·Registered May 12, 2015 – May 12, 2025Cancelled- Analysis ID
- 0d44cc9c420363d5b2ed07f2b946a939
- Customs Code
- DHA09401521400
- Manufacturer
- DYNEX TECHNOLOGIES INC.
- Manufacturer Country
- United States
- Authorized Representative
- Abbott Rapid Diagnostics Health Corp.
- 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
- Input;; QMS/QSD
- Registration Date
- May 12, 2015
- Expiry Date
- May 12, 2025
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Dynex" Disco Clinical Use Enzyme 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 0d44cc9c420363d5b2ed07f2b946a939 and manufactured by DYNEX TECHNOLOGIES INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
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.