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“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.

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9e0eeb8cc96312a4a185fcbff1f08121
Registration Details
Taiwan FDA Registration: 9e0eeb8cc96312a4a185fcbff1f08121
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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

9e0eeb8cc96312a4a185fcbff1f08121

Ministry of Health Medical Device Import No. 033580

DHA05603358004

Company Information

Korea, Republic of

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

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