Taiwan FDA registration 9b96f40f4e6309185466445831e43a77

"Shanmo" AnJie automatic body processing system (unsterilized)

TW: “山默”安傑自動化檢體處理系統 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·THERMO FISHER SCIENTIFIC OY·Registered Oct 01, 2021 – Oct 31, 2024Expired
Registration details
Analysis ID
9b96f40f4e6309185466445831e43a77
Customs Code
DHA08401373802
Company information
Manufacturer Country
Finland
Authorized Representative
DKSH TAIWAN LTD.
Product details
Intended Use
Limited to the first level identification range of the "Individual Photometric Chemistry Analyzer for Clinical Use (A.2160)" of the Measures for the Classification and Grading 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
Oct 01, 2021
Expiry Date
Oct 31, 2024
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About this record

Access comprehensive regulatory information for "Shanmo" AnJie automatic body processing system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9b96f40f4e6309185466445831e43a77 and manufactured by THERMO FISHER SCIENTIFIC OY. The authorized representative in Taiwan is DKSH TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including THERMO FISHER SCIENTIFIC OY, 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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