Taiwan FDA registration ba298c729e7d0a4f24c5b0825911722d
“YERIM” Q-Switched Nd:YAG Laser System
TW: “藝林”Q開關釹雅各雷射系統
Taiwan·Risk Class 2·MD·Yerim Engineering Co., Ltd.·Registered Sep 20, 2017 – Sep 20, 2022ExpiredRegistration details
- Analysis ID
- ba298c729e7d0a4f24c5b0825911722d
- License Form
- Ministry of Health Medical Device Import No. 030240
- Customs Code
- DHA05603024004
Company information
- Manufacturer
- Yerim Engineering Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- K2 INTERNATIONAL MEDICAL INC.
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
- Sep 20, 2017
- Expiry Date
- Sep 20, 2022
About this record
Access comprehensive regulatory information for “YERIM” Q-Switched Nd:YAG Laser System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba298c729e7d0a4f24c5b0825911722d and manufactured by Yerim Engineering Co., Ltd.. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL INC..
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