Taiwan FDA registration 87d1d8fbd87450cd2e9e64e7e220562c

“Jeisys” LinearFirm Focused Ultrasound System

TW: “婕希"立線聚焦超音波系統
Taiwan flagTaiwan·Risk Class 2·MD·Jeisys Medical Inc.·Registered Apr 18, 2019 – Apr 18, 2024Expired
Registration details
Analysis ID
87d1d8fbd87450cd2e9e64e7e220562c
License Form
Ministry of Health Medical Device Import No. 032512
Customs Code
DHA05603251208
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
Taike Medical Technology 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
Dates and status
Registration Date
Apr 18, 2019
Expiry Date
Apr 18, 2024
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About this record

Access comprehensive regulatory information for “Jeisys” LinearFirm 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 87d1d8fbd87450cd2e9e64e7e220562c and manufactured by Jeisys Medical Inc.. The authorized representative in Taiwan is Taike Medical Technology 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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