Taiwan FDA registration 916012395dbc6c23d14ee418d43b3acc
Anres laser therapy device
TW: 安雷斯雷射治療儀
Registration details
- Analysis ID
- 916012395dbc6c23d14ee418d43b3acc
- Customs Code
- DHY00500357407
Company information
- Manufacturer
- KONFTEC CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- KONFTEC CORPORATION
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.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- Domestic
Dates and status
- Registration Date
- Feb 06, 2012
- Expiry Date
- Feb 06, 2027
About this record
Access comprehensive regulatory information for Anres laser therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 916012395dbc6c23d14ee418d43b3acc and manufactured by KONFTEC CORPORATION. The authorized representative in Taiwan is KONFTEC CORPORATION.
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