"Gosden Dynos" Thunder Immunity Analyzer (Unsterilized)
- Analysis ID
- d14c7255912199fc77e798c63b9d76f5
- Customs Code
- DHA09401631406
- Manufacturer
- GOLD STANDARD DIAGNOSTICS CORP.
- 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
- Mar 24, 2016
- Expiry Date
- Mar 24, 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 "Gosden Dynos" Thunder Immunity 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 d14c7255912199fc77e798c63b9d76f5 and manufactured by GOLD STANDARD DIAGNOSTICS CORP.. 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 GOLD STANDARD DIAGNOSTICS CORP., 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.