Taiwan FDA registration d98338581a453d8a4df60c71900f2dc7

"Reesan" Desktop Automatic Chemical Cold Light Immunoassay Analyzer (Unsterilized)

TW: "禮雅尚" 桌上型全自動化學冷光免疫分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·DIASORIN S.P.A.·Registered Jan 22, 2021 – Jan 22, 2026Cancelled
Registration details
Analysis ID
d98338581a453d8a4df60c71900f2dc7
Customs Code
DHA09402226900
Company information
Manufacturer
DIASORIN S.P.A.
Manufacturer Country
Italy
Authorized Representative
MEDRICH INSTRUMENT CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Jan 22, 2021
Expiry Date
Jan 22, 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 "Reesan" Desktop Automatic Chemical Cold Light Immunoassay 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 d98338581a453d8a4df60c71900f2dc7 and manufactured by DIASORIN S.P.A.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..

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