Taiwan FDA registration 6b25e4ba72e1ba93f57885dd159b4d63
"Clear flow" Bantflorian percutaneous puncture angioplasty catheter
TW: “清流”班特弗洛里安經皮穿刺血管成形術導管
Taiwan·Risk Class 2·CLEARSTREAM TECHNOLOGIES LTD.·Registered Nov 05, 2012 – Nov 05, 2017CancelledRegistration details
- Analysis ID
- 6b25e4ba72e1ba93f57885dd159b4d63
- Customs Code
- DHA00602415702
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 Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Nov 05, 2012
- Expiry Date
- Nov 05, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Clear flow" Bantflorian percutaneous puncture angioplasty catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6b25e4ba72e1ba93f57885dd159b4d63 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