Taiwan FDA registration 628760d298eb6a177e5da4c066bcb19d
"Koster" Uticy third generation ultrasonic probe
TW: “寇斯特”優緹偲第三代超音波探頭
Registration details
- Analysis ID
- 628760d298eb6a177e5da4c066bcb19d
- Customs Code
- DHA05603459101
Company information
- Manufacturer
- KORUST Co., Ltd.;; Diamond Biomedical Co., Ltd
- Manufacturer Country
- Taiwan, Province of China;;Korea, Republic of
- Authorized Representative
- DIAMOND BIOTECHNOLOGY 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)
- I.4590 Focused Ultrasound Stimulator
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Jun 08, 2021
- Expiry Date
- Jun 08, 2026
About this record
Access comprehensive regulatory information for "Koster" Uticy third generation ultrasonic probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 628760d298eb6a177e5da4c066bcb19d and manufactured by KORUST Co., Ltd.;; Diamond Biomedical Co., Ltd. The authorized representative in Taiwan is DIAMOND BIOTECHNOLOGY 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