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“DAESUNG” Air compression therapy system - Taiwan Registration 1306e4f04665b2fd583cf6f70b9b5d8b

Access comprehensive regulatory information for “DAESUNG” Air compression therapy system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1306e4f04665b2fd583cf6f70b9b5d8b 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.

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1306e4f04665b2fd583cf6f70b9b5d8b
Registration Details
Taiwan FDA Registration: 1306e4f04665b2fd583cf6f70b9b5d8b
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Device Details

“DAESUNG” Air compression therapy system
TW: “大新”肢體按摩器
Risk Class 2
MD

Registration Details

1306e4f04665b2fd583cf6f70b9b5d8b

Ministry of Health Medical Device Import No. 028154

DHA05602815406

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

Jan 22, 2016

Jan 22, 2026