Pure Global

“DAESUNG”Intermittent Pneumatic Compression System - Taiwan Registration 330af9b583a91faa716041017b97859b

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 330af9b583a91faa716041017b97859b 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. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
330af9b583a91faa716041017b97859b
Registration Details
Taiwan FDA Registration: 330af9b583a91faa716041017b97859b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

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

Registration Details

330af9b583a91faa716041017b97859b

Ministry of Health Medical Device Import No. 035796

DHA05603579601

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

o Physical Medical Sciences

O5650 Power Expansion Tubular Massager

Imported from abroad

Dates and Status

Sep 18, 2022

Sep 18, 2027