Taiwan FDA registration ac149fc6f6296279835cc5c44f474884
"Clear Stream" Rex percutaneous puncture angioplasty catheter
TW: “清流”銳克斯經皮穿刺血管成形術導管
Taiwan·Risk Class 2·CLEARSTREAM TECHNOLOGIES LTD.·Registered Nov 05, 2012 – Nov 05, 2022CancelledRegistration details
- Analysis ID
- ac149fc6f6296279835cc5c44f474884
- Customs Code
- DHA00602415600
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, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Clear Stream" Rex 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 ac149fc6f6296279835cc5c44f474884 and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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