"Ruibang Biomedical" Lemp fluorescence analyzer (unsterilized) - Taiwan Registration 56539d6b6c7d768d114a0beaee84a6e5
Access comprehensive regulatory information for "Ruibang Biomedical" Lemp 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 56539d6b6c7d768d114a0beaee84a6e5 and manufactured by RESPONSE BIOMEDICAL CORPORATION. The authorized representative in Taiwan is RECHI CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RESPONSE BIOMEDICAL CORPORATION, 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.
Device Details
Product Details
Limited to the classification and grading management measures of medical equipment "fluorescence instrument for clinical use (A.2560)" the first level identification range.
A Clinical chemistry and clinical toxicology
A.2560 Fluorometer for clinical use
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Oct 01, 2021
Oct 31, 2025