Taiwan FDA registration 0dbddf98be7a721d3d98f8bbceb9b3a6

"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 Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
0dbddf98be7a721d3d98f8bbceb9b3a6
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 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
國產;; QMS/QSD
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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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 0dbddf98be7a721d3d98f8bbceb9b3a6 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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