Taiwan FDA registration 9de060b58ad07ff99f920f1efa26179f
“Jeisys” Nd:YAG Laser Surgical Unit
TW: “婕曦”銣雅克雷射
Taiwan·Risk Class 2·MD·Jeisys Medical Inc.·Registered Jun 13, 2013 – Jun 13, 2028ActiveRegistration details
- Analysis ID
- 9de060b58ad07ff99f920f1efa26179f
- License Form
- Department of Health Medical Device Import No. 025117
- Customs Code
- DHA00602511705
Company information
- Manufacturer
- Jeisys Medical Inc.
- 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)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 13, 2013
- Expiry Date
- Jun 13, 2028
About this record
Access comprehensive regulatory information for “Jeisys” Nd:YAG Laser 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 9de060b58ad07ff99f920f1efa26179f and manufactured by Jeisys Medical Inc.. The authorized representative in Taiwan is YUNGLIN BIOTECHNOLOGY CO., LTD..
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