Taiwan FDA registration 5820212732ac611c6cd1555ca99f6d8d
"Clear stream" Qingpai European-American plus percutaneous puncture angioplasty catheter
TW: “清流”清派歐美加經皮穿刺血管成形術導管
Taiwan·Risk Class 2·CLEARSTREAM TECHNOLOGIES LTD.·Registered Nov 08, 2012 – Nov 08, 2017CancelledRegistration details
- Analysis ID
- 5820212732ac611c6cd1555ca99f6d8d
- Customs Code
- DHA00602416103
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 08, 2012
- Expiry Date
- Nov 08, 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 stream" Qingpai European-American plus 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 5820212732ac611c6cd1555ca99f6d8d and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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