Taiwan FDA registration c7a2474b96bed1730c9b0251aa82eb26

"Gosden Dynos" Thunder Immunity Analyzer (Unsterilized)

TW: "高司登戴諾斯" 雷霆免疫分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·GOLD STANDARD DIAGNOSTICS CORP.·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
c7a2474b96bed1730c9b0251aa82eb26
Customs Code
DHA08401631400
Company information
Manufacturer Country
United States
Authorized Representative
Abbott Rapid Diagnostics Health Corp.
Product details
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
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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About this record

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 c7a2474b96bed1730c9b0251aa82eb26 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.

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