"Dinax" Diess Clinical use enzyme analyzer (unsterilized)
Taiwan·Risk Class 1·DYNEX TECHNOLOGIES INC.·Registered Mar 22, 2013 – Mar 22, 2023Cancelled- Analysis ID
- 30ee8748dff6cd951b5cea3e379a69fc
- Customs Code
- DHA04401283100
- 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
- QMS/QSD;; 輸入
- Registration Date
- Mar 22, 2013
- Expiry Date
- Mar 22, 2023
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Dinax" Diess 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 30ee8748dff6cd951b5cea3e379a69fc 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.