Taiwan FDA registration 09cd9ac77b69af105d9f471a901c95eb
"Taiyu" focuses on ultrasound therapy systems
TW: “太宇”聚焦超音波治療系統
Taiwan·Risk Class 2·DAEJU MEDITECH ENGINEERING·Registered Oct 03, 2017 – Jan 04, 2022CancelledRegistration details
- Analysis ID
- 09cd9ac77b69af105d9f471a901c95eb
- Customs Code
- DHA05602924300
Company information
- Manufacturer
- DAEJU MEDITECH ENGINEERING
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- YUNGLIN BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4590 Focused Ultrasound Stimulator
- Import Information
- Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
Dates and status
- Registration Date
- Oct 03, 2017
- Expiry Date
- Jan 04, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Taiyu" focuses on ultrasound therapy systems in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 09cd9ac77b69af105d9f471a901c95eb and manufactured by DAEJU MEDITECH ENGINEERING. The authorized representative in Taiwan is YUNGLIN BIOTECHNOLOGY CO., LTD..
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