Taiwan FDA registration 923f391d3784ec1d27756001b3874d9f
"Powerway" surgical electrocautery
TW: "保威" 手術電燒刀
Registration details
- Analysis ID
- 923f391d3784ec1d27756001b3874d9f
- Customs Code
- DHA00601190606
Company information
- Manufacturer
- Bovie Medical Corporation
- Manufacturer Country
- United States
- Authorized Representative
- KINGJING INTERNATIONAL CO., LTD.
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
- Import Information
- import
Dates and status
- Registration Date
- Sep 13, 2005
- Expiry Date
- Sep 13, 2025
About this record
Access comprehensive regulatory information for "Powerway" surgical electrocautery in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 923f391d3784ec1d27756001b3874d9f and manufactured by Bovie Medical Corporation. The authorized representative in Taiwan is KINGJING INTERNATIONAL CO., LTD..
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