Taiwan FDA registration 34e0739db191a5e4f0fb1e6d1f41a5f4
“ClearStream” ReeFlex PTA Catheter
TW: “清流”銳弗斯經皮穿刺血管成形術導管
Taiwan·Risk Class 2·MD·CLEARSTREAM TECHNOLOGIES LTD.·Registered Feb 17, 2014 – Feb 17, 2019CancelledRegistration details
- Analysis ID
- 34e0739db191a5e4f0fb1e6d1f41a5f4
- License Form
- Ministry of Health Medical Device Import No. 025814
- Customs Code
- DHA05602581407
Company information
- Manufacturer
- CLEARSTREAM TECHNOLOGIES LTD.
- Manufacturer Country
- Ireland
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 17, 2014
- Expiry Date
- Feb 17, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for “ClearStream” ReeFlex PTA Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 34e0739db191a5e4f0fb1e6d1f41a5f4 and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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