Taiwan FDA registration 0fcba6f1af7dce7f2c7631c93bfdad26
"Clear stream" Bante Alfa percutaneous puncture angioplasty catheter
TW: “清流”班特阿爾發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
- 0fcba6f1af7dce7f2c7631c93bfdad26
- Customs Code
- DHA00602415508
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" Bante Alfa 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 0fcba6f1af7dce7f2c7631c93bfdad26 and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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