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“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.

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d83098e151426bc4d2a6c9ef1dd20aae
Registration Details
Taiwan FDA Registration: d83098e151426bc4d2a6c9ef1dd20aae
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Device Details

“DAESUNG” Intermittent Pneumatic Compression System
TW: “大新”間歇充氣加壓系統
Risk Class 2
MD

Registration Details

d83098e151426bc4d2a6c9ef1dd20aae

Ministry of Health Medical Device Import No. 029773

DHA05602977300

Company Information

Korea, Republic of

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

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