Taiwan FDA registration 5deb8ddc5d87c52bb66892e6a29785ab
“Cordis” Sleek 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 Sep 30, 2013 – Sep 30, 2023ExpiredRegistration details
- Analysis ID
- 5deb8ddc5d87c52bb66892e6a29785ab
- License Form
- Ministry of Health Medical Device Import No. 025249
- Customs Code
- DHA05602524902
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
- Sep 30, 2013
- Expiry Date
- Sep 30, 2023
About this record
Access comprehensive regulatory information for “Cordis” Sleek 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 5deb8ddc5d87c52bb66892e6a29785ab and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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