Taiwan FDA registration 63435cc0d17b4eb72c80cb2a9980db4e
“RF” ablation system and Accessories
TW: “艾爾發”電子燒灼機及其附件
Taiwan·Risk Class 2·MD·RF MEDICAL CO., LTD·Registered Mar 15, 2017 – Mar 15, 2022ExpiredRegistration details
- Analysis ID
- 63435cc0d17b4eb72c80cb2a9980db4e
- License Form
- Ministry of Health Medical Device Import No. 029602
- Customs Code
- DHA05602960202
Company information
- Manufacturer
- RF MEDICAL CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- GOLEAD BIOPHARM INC.
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)
- I4400 Electric knife for cutting and hemostasis and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 15, 2017
- Expiry Date
- Mar 15, 2022
About this record
Access comprehensive regulatory information for “RF” ablation system and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 63435cc0d17b4eb72c80cb2a9980db4e and manufactured by RF MEDICAL CO., LTD. The authorized representative in Taiwan is GOLEAD BIOPHARM INC..
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