Taiwan FDA registration 330af9b583a91faa716041017b97859b
“DAESUNG”Intermittent Pneumatic Compression System
TW: “大新”間歇充氣加壓系統
Taiwan·Risk Class 2·MD·DAESUNG MAREF CO., LTD.·Registered Sep 18, 2022 – Sep 18, 2027ActiveRegistration details
- Analysis ID
- 330af9b583a91faa716041017b97859b
- License Form
- Ministry of Health Medical Device Import No. 035796
- Customs Code
- DHA05603579601
Company information
- Manufacturer
- DAESUNG MAREF CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- GIGA MEDICAL INSTRUMENT LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O5650 Power Expansion Tubular Massager
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 18, 2022
- Expiry Date
- Sep 18, 2027
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 330af9b583a91faa716041017b97859b and manufactured by DAESUNG MAREF CO., LTD.. The authorized representative in Taiwan is GIGA MEDICAL INSTRUMENT LTD..
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