Taiwan FDA registration dc269f0ac588f95fd3d800ba0b9733ed
“ClearStream” Bard LifeStream Balloon Expandable Vascular Covered Stent
TW: “清流”巴德萊弗司球囊擴張血管覆膜支架
Taiwan·Risk Class 3·MD·CLEARSTREAM TECHNOLOGIES LTD.·Registered Mar 23, 2016 – Mar 23, 2026ExpiredRegistration details
- Analysis ID
- dc269f0ac588f95fd3d800ba0b9733ed
- License Form
- Ministry of Health Medical Device Import No. 028268
- Customs Code
- DHA05602826808
Company information
- Manufacturer
- CLEARSTREAM TECHNOLOGIES LTD.
- Manufacturer Country
- Ireland
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
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)
- E0001 Cardiovascular stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 23, 2016
- Expiry Date
- Mar 23, 2026
About this record
Access comprehensive regulatory information for “ClearStream” Bard LifeStream Balloon Expandable Vascular Covered Stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number dc269f0ac588f95fd3d800ba0b9733ed and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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