“DAESUNG” Intermittent Pneumatic Compression System - Taiwan Registration d83098e151426bc4d2a6c9ef1dd20aae
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 d83098e151426bc4d2a6c9ef1dd20aae 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
d83098e151426bc4d2a6c9ef1dd20aae
Ministry of Health Medical Device Import No. 029773
DHA05602977300
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular devices
E5800 Compression sleeve for extremities
Imported from abroad
Dates and Status
May 26, 2017
May 26, 2027

