Taiwan FDA registration 9e2ea8b02b4f79f0e710905839c33b2f
"Stryker" Cardille Remote Guided Catheter
TW: “史賽克”卡得樂遠端引導導管
Taiwan·Risk Class 2·Stryker Neurovascular·Registered Jul 31, 2017 – Jul 31, 2027ActiveRegistration details
- Analysis ID
- 9e2ea8b02b4f79f0e710905839c33b2f
- Customs Code
- DHA05602999100
Company information
- Manufacturer
- Stryker Neurovascular
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
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
- Jul 31, 2017
- Expiry Date
- Jul 31, 2027
About this record
Access comprehensive regulatory information for "Stryker" Cardille Remote Guided Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e2ea8b02b4f79f0e710905839c33b2f and manufactured by Stryker Neurovascular. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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