Taiwan FDA registration 9e0eeb8cc96312a4a185fcbff1f08121

“DAESUNG” Intermittent Pneumatic Compression System

TW: “大新”間歇充氣加壓系統
Taiwan flagTaiwan·Risk Class 2·MD·DAESUNG MAREF CO., LTD.·Registered May 01, 2020 – May 01, 2025Expired
Registration details
Analysis ID
9e0eeb8cc96312a4a185fcbff1f08121
License Form
Ministry of Health Medical Device Import No. 033580
Customs Code
DHA05603358004
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
GIGA MEDICAL INSTRUMENT LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O5650 Power Expansion Tubular Massager
Import Information
Imported from abroad
Dates and status
Registration Date
May 01, 2020
Expiry Date
May 01, 2025
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About this record

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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