Taiwan FDA registration a02e80f86c9dcd9085985b51cac4812b
"Jessie" electroknife system
TW: “婕曦”電刀系統
Registration details
- Analysis ID
- a02e80f86c9dcd9085985b51cac4812b
- Customs Code
- DHA05602902704
Company information
- Manufacturer
- Jeisys Medical Inc.
- 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, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4400 Cutting and hemostasis electric knives and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- Nov 10, 2016
- Expiry Date
- Nov 10, 2026
About this record
Access comprehensive regulatory information for "Jessie" electroknife system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a02e80f86c9dcd9085985b51cac4812b 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. 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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