Taiwan FDA registration d83098e151426bc4d2a6c9ef1dd20aae

“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 26, 2017 – May 26, 2027Active
Registration details
Analysis ID
d83098e151426bc4d2a6c9ef1dd20aae
License Form
Ministry of Health Medical Device Import No. 029773
Customs Code
DHA05602977300
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)
E Cardiovascular devices
Product Type (Level 2)
E5800 Compression sleeve for extremities
Import Information
Imported from abroad
Dates and status
Registration Date
May 26, 2017
Expiry Date
May 26, 2027
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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 d83098e151426bc4d2a6c9ef1dd20aae and manufactured by DAESUNG MAREF CO., LTD.. The authorized representative in Taiwan is GIGA MEDICAL INSTRUMENT LTD..

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