Taiwan FDA registration 5ba78f9e19b87baaff85cac1ddd1aad6
“G.N.S” neoV Diode Laser Family
TW: “吉恩司”二極體雷射
Taiwan·Risk Class 2·MD·G.N.S neoLaser Ltd·Registered Apr 12, 2018 – Apr 12, 2028ActiveRegistration details
- Analysis ID
- 5ba78f9e19b87baaff85cac1ddd1aad6
- License Form
- Ministry of Health Medical Device Import No. 031028
- Customs Code
- DHA05603102801
Company information
- Manufacturer
- G.N.S neoLaser Ltd
- Manufacturer Country
- Israel
- Authorized Representative
- GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH
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
- Apr 12, 2018
- Expiry Date
- Apr 12, 2028
About this record
Access comprehensive regulatory information for “G.N.S” neoV Diode Laser Family in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5ba78f9e19b87baaff85cac1ddd1aad6 and manufactured by G.N.S neoLaser Ltd. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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