Taiwan FDA registration 729e36cbccc1b00002c41e48d9891271
“RF” Electrocautery System Generator
TW: “睿孚”射頻電燒儀
Taiwan·Risk Class 2·MD·RF Medical Co., Ltd.·Registered Jul 29, 2021 – Jul 29, 2026ExpiredRegistration details
- Analysis ID
- 729e36cbccc1b00002c41e48d9891271
- License Form
- Ministry of Health Medical Device Import No. 034259
- Customs Code
- DHA05603425906
Company information
- Manufacturer
- RF Medical Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4400 Electric knife for cutting and hemostasis and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 29, 2021
- Expiry Date
- Jul 29, 2026
About this record
Access comprehensive regulatory information for “RF” Electrocautery System Generator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 729e36cbccc1b00002c41e48d9891271 and manufactured by RF Medical Co., Ltd.. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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