Taiwan FDA registration 1e73d80a4efe18113683ca61a2b8fcd9
“Stryker” Surpass Evolve Flow Diverter System
TW: “史賽克”充沛流量導引套
Taiwan·Risk Class 3·MD·Stryker Neurovascular·Registered Feb 06, 2021 – Feb 06, 2026ExpiredRegistration details
- Analysis ID
- 1e73d80a4efe18113683ca61a2b8fcd9
- License Form
- Ministry of Health Medical Device Import No. 034283
- Customs Code
- DHA05603428303
Company information
- Manufacturer
- Stryker Neurovascular
- Manufacturer Country
- Ireland
- 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)
- K5950 Artificial embolization device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 06, 2021
- Expiry Date
- Feb 06, 2026
About this record
Access comprehensive regulatory information for “Stryker” Surpass Evolve Flow Diverter System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1e73d80a4efe18113683ca61a2b8fcd9 and manufactured by Stryker Neurovascular. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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