"Pusen" Qiwei Clinical use enzyme analyzer (unsterilized)
Taiwan·Risk Class 1·DYNEX TECHNOLOGIES INC.·Registered Oct 01, 2021 – Oct 31, 2024Expired- Analysis ID
- 1f04d48a32be9bd867124a25b987715d
- Customs Code
- DHA08401347200
- Manufacturer
- DYNEX TECHNOLOGIES INC.
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
- 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
- Oct 01, 2021
- Expiry Date
- Oct 31, 2024
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Access comprehensive regulatory information for "Pusen" Qiwei 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 1f04d48a32be9bd867124a25b987715d and manufactured by DYNEX TECHNOLOGIES INC.. The authorized representative in Taiwan is GENERAL BIOLOGICALS 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.