Taiwan FDA registration 4a35ac9f785e24356e24d0b1b0081d2c
“Cambridge” CRF Radiofrequency Ablation System
TW: “康橋”射頻消融手術電刀系統
Taiwan·Risk Class 2·MD·Cambridge Interventional LLC·Registered Jun 10, 2022 – Jun 10, 2027ActiveRegistration details
- Analysis ID
- 4a35ac9f785e24356e24d0b1b0081d2c
- License Form
- Ministry of Health Medical Device Import No. 035574
- Customs Code
- DHA05603557406
Company information
- Manufacturer
- Cambridge Interventional LLC
- Manufacturer Country
- United States
- Authorized Representative
- KROMAX INTERNATIONAL CORP.
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 10, 2022
- Expiry Date
- Jun 10, 2027
About this record
Access comprehensive regulatory information for “Cambridge” CRF Radiofrequency Ablation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4a35ac9f785e24356e24d0b1b0081d2c and manufactured by Cambridge Interventional LLC. The authorized representative in Taiwan is KROMAX INTERNATIONAL CORP..
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