Taiwan FDA registration e93a549f66c7bbced796bcda322fb869
“GTG” Semi-conductor Laser Unit
TW: “吉特”二極體雷射
Taiwan·Risk Class 2·MD·GTG WELLNESS CO., LTD·Registered Mar 01, 2017 – Mar 01, 2022ExpiredRegistration details
- Analysis ID
- e93a549f66c7bbced796bcda322fb869
- License Form
- Ministry of Health Medical Device Import No. 029470
- Customs Code
- DHA05602947008
Company information
- Manufacturer
- GTG WELLNESS CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MAVIS MEDICAL ENTERPRISE 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; The use of this equipment shall comply with the "Administrative Measures for the Implementation or Use of Specific Medical Technical Examination and Inspection Medical Equipment"
Dates and status
- Registration Date
- Mar 01, 2017
- Expiry Date
- Mar 01, 2022
About this record
Access comprehensive regulatory information for “GTG” Semi-conductor Laser Unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e93a549f66c7bbced796bcda322fb869 and manufactured by GTG WELLNESS CO., LTD. The authorized representative in Taiwan is MAVIS MEDICAL ENTERPRISE 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.
Free DatabasePowered by Pure Global AI89,000+ Devices