Taiwan FDA registration 8152c6ba668b4880119bd632be93d248
“BIOTRONIK” 3Flow Aspiration Catheter
TW: “百多力”抽吸導管
Taiwan·Risk Class 2·MD·ARTHESYS·Registered Sep 25, 2020 – Sep 25, 2025ExpiredRegistration details
- Analysis ID
- 8152c6ba668b4880119bd632be93d248
- License Form
- Ministry of Health Medical Device Import No. 033963
- Customs Code
- DHA05603396307
Company information
- Manufacturer
- ARTHESYS
- Manufacturer Country
- France
- 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)
- E5150 Thrombectomy catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 25, 2020
- Expiry Date
- Sep 25, 2025
About this record
Access comprehensive regulatory information for “BIOTRONIK” 3Flow Aspiration Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8152c6ba668b4880119bd632be93d248 and manufactured by ARTHESYS. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.
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