Taiwan FDA registration f954bf8f546ef6ea1587ea4582e30628
"Koster" Utyss system
TW: “寇斯特”優提斯系統
Taiwan·Risk Class 2·KORUST Co., Ltd.·Registered Sep 27, 2018 – Sep 27, 2028ActiveRegistration details
- Analysis ID
- f954bf8f546ef6ea1587ea4582e30628
- Customs Code
- DHA05603164509
Company information
- Manufacturer
- KORUST Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- DIAMOND 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
- Sep 27, 2018
- Expiry Date
- Sep 27, 2028
About this record
Access comprehensive regulatory information for "Koster" Utyss system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f954bf8f546ef6ea1587ea4582e30628 and manufactured by KORUST Co., Ltd.. The authorized representative in Taiwan is DIAMOND BIOTECHNOLOGY CO., LTD..
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