Taiwan FDA registration 6f06963bc79f963a6c74306e89b539bc

"Jeisys" LIPOcel Focused Ultrasound System

TW: "婕曦" 立倍塑聚焦超音波系統
Taiwan flagTaiwan·Risk Class 2·MD·Jeisys Medical Inc.·Registered Jul 04, 2017 – Jul 04, 2027Active
Registration details
Analysis ID
6f06963bc79f963a6c74306e89b539bc
License Form
Ministry of Health Medical Device Import No. 029925
Customs Code
DHA05602992500
Company information
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 and plastic surgical devices
Product Type (Level 2)
I4590 Focused Ultrasound Stimulator
Import Information
Imported from abroad; The use of this equipment shall comply with the "Administrative Measures for the Implementation or Use of Specific Medical Technical Examination and Inspection Medical Equipment"
Dates and status
Registration Date
Jul 04, 2017
Expiry Date
Jul 04, 2027
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About this record

Access comprehensive regulatory information for "Jeisys" LIPOcel Focused Ultrasound System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6f06963bc79f963a6c74306e89b539bc and manufactured by Jeisys Medical Inc.. The authorized representative in Taiwan is YUNGLIN BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Jeisys Medical Inc., and 1 recent registrations in the same category. 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.

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