Taiwan FDA registration 309c50cbcd661333991250ea86fbafee
“Stryker” Trevo Microcatheter
TW: “史賽克” 崔佛微型導管
Taiwan·Risk Class 2·MD·Stryker Neurovascular·Registered Sep 15, 2014 – Sep 15, 2024ExpiredRegistration details
- Analysis ID
- 309c50cbcd661333991250ea86fbafee
- License Form
- Ministry of Health Medical Device Import No. 026563
- Customs Code
- DHA05602656300
Company information
- Manufacturer
- Stryker Neurovascular
- Manufacturer Country
- 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 devices
- Product Type (Level 2)
- E1200 Diagnostic endovascular catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 15, 2014
- Expiry Date
- Sep 15, 2024
About this record
Access comprehensive regulatory information for “Stryker” Trevo Microcatheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 309c50cbcd661333991250ea86fbafee and manufactured by Stryker Neurovascular. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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