Taiwan FDA registration e2287868ee1135456282e369da1d98f3
“Cordis” Sleek OTW Percutaneous Transluminal Angioplasty (PTA) Catheter
TW: “考迪斯”速立刻擴張導管
Taiwan·Risk Class 2·MD·CLEARSTREAM TECHNOLOGIES LTD.·Registered Jun 26, 2014 – Jun 26, 2024ExpiredRegistration details
- Analysis ID
- e2287868ee1135456282e369da1d98f3
- License Form
- Ministry of Health Medical Device Import No. 026374
- Customs Code
- DHA05602637400
Company information
- Manufacturer
- CLEARSTREAM TECHNOLOGIES LTD.
- Manufacturer Country
- Ireland
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 26, 2014
- Expiry Date
- Jun 26, 2024
About this record
Access comprehensive regulatory information for “Cordis” Sleek OTW Percutaneous Transluminal Angioplasty (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 e2287868ee1135456282e369da1d98f3 and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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