Taiwan FDA registration f153e980f56d7f5846a1cbb40b1d86c4
“Stryker” Distal Access Catheter
TW: “史賽克”遠端輔助導管
Taiwan·Risk Class 2·MD·Stryker Neurovascular·Registered Nov 17, 2014 – Nov 17, 2019CancelledRegistration details
- Analysis ID
- f153e980f56d7f5846a1cbb40b1d86c4
- License Form
- Ministry of Health Medical Device Import No. 026678
- Customs Code
- DHA05602667804
Company information
- Manufacturer
- Stryker Neurovascular
- Manufacturer Country
- United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
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
- Nov 17, 2014
- Expiry Date
- Nov 17, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Stryker” Distal Access Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f153e980f56d7f5846a1cbb40b1d86c4 and manufactured by Stryker Neurovascular. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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