Taiwan FDA registration 9680f90b19c1f112efcbb70920932928
“ENDOVISION” Radiofrequency Plasma Electrosurgical system
TW: “恩多威視”手術用電燒刀系統
Taiwan·Risk Class 2·MD·ENDOVISION CO., LTD·Registered Jun 26, 2023 – Jun 26, 2028ActiveRegistration details
- Analysis ID
- 9680f90b19c1f112efcbb70920932928
- License Form
- Ministry of Health Medical Device Import No. 036655
- Customs Code
- DHA05603665501
Company information
- Manufacturer
- ENDOVISION CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- BAUI BIOTECH CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4400 Electric knife for cutting and hemostasis and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 26, 2023
- Expiry Date
- Jun 26, 2028
About this record
Access comprehensive regulatory information for “ENDOVISION” Radiofrequency Plasma Electrosurgical system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9680f90b19c1f112efcbb70920932928 and manufactured by ENDOVISION CO., LTD. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..
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