"DSmedi" Plinth (Non-Sterile) - Taiwan Registration 55d034bae9a09db72c44308e6ea71033
Access comprehensive regulatory information for "DSmedi" Plinth (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 55d034bae9a09db72c44308e6ea71033 and manufactured by DSMEDI, INC.. The authorized representative in Taiwan is HABITZ MEDTECH CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DSMEDI, INC., 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
Registration Details
55d034bae9a09db72c44308e6ea71033
Ministry of Health Medical Device Import Registration No. 022340
DHA08402234000
Product Details
Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Treatment Table (O.3520)".
o Equipment for physical medicine
O3520 treatment unit
Imported from abroad
Dates and Status
Oct 01, 2021
Oct 31, 2026