“DAESUNG” Intermittent Pneumatic Compression System - Taiwan Registration 9e0eeb8cc96312a4a185fcbff1f08121
Access comprehensive regulatory information for “DAESUNG” Intermittent Pneumatic Compression System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e0eeb8cc96312a4a185fcbff1f08121 and manufactured by DAESUNG MAREF CO., LTD.. The authorized representative in Taiwan is GIGA MEDICAL INSTRUMENT LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DAESUNG MAREF 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.
Device Details
Registration Details
9e0eeb8cc96312a4a185fcbff1f08121
Ministry of Health Medical Device Import No. 033580
DHA05603358004
Product Details
For details, it is Chinese approved copy of the imitation order
o Equipment for physical medicine
O5650 Power Expansion Tubular Massager
Imported from abroad
Dates and Status
May 01, 2020
May 01, 2025

