LUMIPULSE G1200 (Non-Sterile) - Taiwan Registration 2c2cb8996b9a5a5c711949be0c85d669
Access comprehensive regulatory information for LUMIPULSE G1200 (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2c2cb8996b9a5a5c711949be0c85d669 and manufactured by OTSUKA ELECTRONICS CO., LTD. SHIGA FACTORY. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical Co., Ltd.
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.
Device Details
Registration Details
2c2cb8996b9a5a5c711949be0c85d669
Ministry of Health Medical Device Import Registration No. 009828
DHA08400982801
Product Details
A Clinical chemistry and clinical toxicology
A2160 Individual photometric chemistry analyzer for clinical use
Imported from abroad
Dates and Status
Oct 01, 2021
Oct 31, 2026
Oct 28, 2022
Cancellation Information
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