Taiwan FDA registration dbe637011c94e9d2a31e22a3bd10259b
“CardioFocus” HeartLight Endoscopic Ablation System
TW: “福客星”朗光內視鏡消融系統
Taiwan·Risk Class 3·MD·CardioFocus, Inc.·Registered Aug 07, 2020 – Aug 07, 2025ExpiredRegistration details
- Analysis ID
- dbe637011c94e9d2a31e22a3bd10259b
- License Form
- Ministry of Health Medical Device Import No. 033810
- Customs Code
- DHA05603381008
Company information
- Manufacturer
- CardioFocus, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- LORION ENTERPRISES INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E0008 Percutaneous puncture of cardiac ablation system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 07, 2020
- Expiry Date
- Aug 07, 2025
About this record
Access comprehensive regulatory information for “CardioFocus” HeartLight Endoscopic Ablation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number dbe637011c94e9d2a31e22a3bd10259b and manufactured by CardioFocus, Inc.. The authorized representative in Taiwan is LORION ENTERPRISES INC..
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