"Pusen" Qiwei Clinical use enzyme analyzer (unsterilized)
Taiwan·Risk Class 1·DYNEX TECHNOLOGIES INC.·Registered Oct 02, 2013 – Oct 02, 2023Cancelled- Analysis ID
- 033e6638ca1ee7b79547ec28ac7c4e0a
- Customs Code
- DHA09401347209
- Manufacturer
- DYNEX TECHNOLOGIES INC.
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS 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
- Oct 02, 2013
- Expiry Date
- Oct 02, 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 "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 033e6638ca1ee7b79547ec28ac7c4e0a and manufactured by DYNEX TECHNOLOGIES INC.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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