Taiwan FDA registration 4363cb30949bbc725e334a637ada8ea6

"Xuanjiang" automatic biochemical analyzer (unsterilized)

TW: "朕江" 自動生化分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·LANNER BIOTECHNOLOGY CO., LTD.·Registered Jan 05, 2016 – Jan 05, 2026Cancelled
Registration details
Analysis ID
4363cb30949bbc725e334a637ada8ea6
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
LANNER BIOTECHNOLOGY 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
國產;; QMS/QSD
Dates and status
Registration Date
Jan 05, 2016
Expiry Date
Jan 05, 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 "Xuanjiang" automatic biochemical 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 4363cb30949bbc725e334a637ada8ea6 and manufactured by LANNER BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LANNER BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LANNER BIOTECHNOLOGY CO., LTD., 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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