Taiwan FDA registration 20fae129da59e032bbe952493f99e33a
“Stryker” Trevo ProVue Retriever
TW: “史賽克”崔弗普威取回器
Taiwan·Risk Class 2·MD·Stryker Neurovascular·Registered Apr 27, 2015 – Apr 27, 2025ExpiredRegistration details
- Analysis ID
- 20fae129da59e032bbe952493f99e33a
- License Form
- Ministry of Health Medical Device Import No. 027275
- Customs Code
- DHA05602727500
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)
- K Devices for neuroscience
- Product Type (Level 2)
- K5600 Neurovascular mechanical clot removal device for the treatment of acute ischemic stroke
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 27, 2015
- Expiry Date
- Apr 27, 2025
About this record
Access comprehensive regulatory information for “Stryker” Trevo ProVue Retriever in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 20fae129da59e032bbe952493f99e33a and manufactured by Stryker Neurovascular. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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