Taiwan FDA registration 20c67ef28e7613a37f4186ee4b5858ee

"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 Dec 31, 2013 – Dec 31, 2023Cancelled
Registration details
Analysis ID
20c67ef28e7613a37f4186ee4b5858ee
Customs Code
DHA09401373808
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 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
Input;; QMS/QSD
Dates and status
Registration Date
Dec 31, 2013
Expiry Date
Dec 31, 2023
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 "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 20c67ef28e7613a37f4186ee4b5858ee 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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