Taiwan FDA registration d14c7255912199fc77e798c63b9d76f5

"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 Mar 24, 2016 – Mar 24, 2026Cancelled
Registration details
Analysis ID
d14c7255912199fc77e798c63b9d76f5
Customs Code
DHA09401631406
Company information
Manufacturer Country
United States
Authorized Representative
Abbott Rapid Diagnostics Health Corp.
Product details
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
Dates and status
Registration Date
Mar 24, 2016
Expiry Date
Mar 24, 2026
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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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 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.

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