Taiwan FDA registration 9dcb3545549e0b6d8cc0c39430ac9596
"Clear flow" Bant percutaneous puncture angioplasty catheter
TW: “清流”班特經皮穿刺血管成形術導管
Taiwan·Risk Class 2·CLEARSTREAM TECHNOLOGIES LTD.·Registered Nov 01, 2012 – Nov 01, 2027ActiveRegistration details
- Analysis ID
- 9dcb3545549e0b6d8cc0c39430ac9596
- Customs Code
- DHA00602415202
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 01, 2012
- Expiry Date
- Nov 01, 2027
About this record
Access comprehensive regulatory information for "Clear flow" Bant 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 9dcb3545549e0b6d8cc0c39430ac9596 and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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