Taiwan FDA registration c26ccabe90021e2c63809f078c1a76d9
“DAEJU” Focused Ultrasound Therapeutic System
TW: “大州”聚焦超音波治療系統
Taiwan·Risk Class 2·MD·DAEJU MEDITECH ENGINEERING Co., Ltd.·Registered Sep 27, 2022 – Sep 27, 2027ActiveRegistration details
- Analysis ID
- c26ccabe90021e2c63809f078c1a76d9
- License Form
- Ministry of Health Medical Device Import No. 035911
- Customs Code
- DHA05603591101
Company information
- Manufacturer
- DAEJU MEDITECH ENGINEERING Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Always Medical Co., Ltd
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4590 Focused Ultrasound Stimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 27, 2022
- Expiry Date
- Sep 27, 2027
About this record
Access comprehensive regulatory information for “DAEJU” Focused Ultrasound Therapeutic System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c26ccabe90021e2c63809f078c1a76d9 and manufactured by DAEJU MEDITECH ENGINEERING Co., Ltd.. The authorized representative in Taiwan is Always Medical Co., 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.
Free DatabasePowered by Pure Global AI89,000+ Devices