Taiwan FDA registration c5c63168c07b18225bb8b901dbff17e4

"Eusana" ultrasound therapy device

TW: “優珊納”超音波治療儀

Taiwan·Risk Class 2·Ulthera, Inc.·Registered Sep 12, 2013 – Sep 12, 2028Active

Registration details

Analysis ID: c5c63168c07b18225bb8b901dbff17e4
Customs Code: DHA05602534409

Company information

Manufacturer: Ulthera, Inc.
Manufacturer Country: United States
Authorized Representative: MERZ ASIA PACIFIC PTE. LTD. TAIWAN BRANCH (SINGAPORE)

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order. New Performance: For details, as shown in Chinese copy of the imitation order approved (the original approved copy of the imitation label approved in 102.9.24 is recycled and invalidated), the following blanks.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4590 Focused Ultrasound Stimulator
Import Information: import

Dates and status

Registration Date: Sep 12, 2013
Expiry Date: Sep 12, 2028

About this record

Access comprehensive regulatory information for "Eusana" ultrasound therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c5c63168c07b18225bb8b901dbff17e4 and manufactured by Ulthera, Inc.. The authorized representative in Taiwan is MERZ ASIA PACIFIC PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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