Taiwan FDA registration f97fe977e3527032ca6ba73873b3155c
“ASTERASYS” Liftera-V high intensity focused ultrasound surgical unit
TW: “艾特拉喜”立特拉聚焦超音波
Taiwan·Risk Class 2·MD·ASTERASYS Co., Ltd.·Registered Jul 17, 2021 – Jul 17, 2026ExpiredRegistration details
- Analysis ID
- f97fe977e3527032ca6ba73873b3155c
- License Form
- Ministry of Health Medical Device Import No. 034711
- Customs Code
- DHA05603471101
Company information
- Manufacturer
- ASTERASYS Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- BP BIOTECHNOLOGY COMPANY
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4590 Focused Ultrasound Stimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 17, 2021
- Expiry Date
- Jul 17, 2026
About this record
Access comprehensive regulatory information for “ASTERASYS” Liftera-V high intensity focused ultrasound surgical unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f97fe977e3527032ca6ba73873b3155c and manufactured by ASTERASYS Co., Ltd.. The authorized representative in Taiwan is BP BIOTECHNOLOGY COMPANY.
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