Taiwan FDA registration 373fe19754e1aa0855b9892f13077984
“BIOTRONIK” Qiona Ablation Irrigation Pump incl. Accessories
TW: “百多力”消融灌注幫浦及其配件
Taiwan·Risk Class 2·MD·MOLLER MEDICAL GMBH·Registered Dec 04, 2020 – Dec 04, 2025ExpiredRegistration details
- Analysis ID
- 373fe19754e1aa0855b9892f13077984
- License Form
- Ministry of Health Medical Device Import No. 034205
- Customs Code
- DHA05603420509
Company information
- Manufacturer
- MOLLER MEDICAL GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- BIOTRONIK TAIWAN LIMITED
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
- Dec 04, 2020
- Expiry Date
- Dec 04, 2025
About this record
Access comprehensive regulatory information for “BIOTRONIK” Qiona Ablation Irrigation Pump incl. Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 373fe19754e1aa0855b9892f13077984 and manufactured by MOLLER MEDICAL GMBH. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.
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