Taiwan FDA registration 1306e4f04665b2fd583cf6f70b9b5d8b
“DAESUNG” Air compression therapy system
TW: “大新”肢體按摩器
Taiwan·Risk Class 2·MD·DAESUNG MAREF CO., LTD.·Registered Jan 22, 2016 – Jan 22, 2026ExpiredRegistration details
- Analysis ID
- 1306e4f04665b2fd583cf6f70b9b5d8b
- License Form
- Ministry of Health Medical Device Import No. 028154
- Customs Code
- DHA05602815406
Company information
- Manufacturer
- DAESUNG MAREF CO., LTD.
- 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
- Jan 22, 2016
- Expiry Date
- Jan 22, 2026
About this record
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..
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