Taiwan FDA registration 629152b0372e1d2d620dd950b9e17dcd

"Medical Complete" Judgment Speedy Dispatch Fluorescence Analyzer (Unsterilized)

TW: "醫全" 判速發順通螢光分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Yamura Electric Industry Co.,Ltd.;; LSI Medience Corporation·Registered Aug 04, 2022 – Oct 31, 2024Expired
Registration details
Analysis ID
629152b0372e1d2d620dd950b9e17dcd
Customs Code
DHA084a0009508
Company information
Manufacturer Country
Japan
Authorized Representative
MEDICARE PRODUCTS INC.
Product details
Intended Use
Limited to the classification and grading management measures of medical equipment "fluorescence instrument for clinical use (A.2560)" the first level identification range.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2560 Fluorometer for clinical use
Dates and status
Registration Date
Aug 04, 2022
Expiry Date
Oct 31, 2024
About this record

Access comprehensive regulatory information for "Medical Complete" Judgment Speedy Dispatch Fluorescence 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 629152b0372e1d2d620dd950b9e17dcd and manufactured by Yamura Electric Industry Co.,Ltd.;; LSI Medience Corporation. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..

This page provides complete technical specifications, regulatory compliance details. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices