Taiwan FDA registration c9c30d593c3837387221aa7ae2c03289
“Stryker” Surpass Streamline Flow Diverter
TW: “史賽克”充沛流量導引器
Taiwan·Risk Class 3·MD·Stryker Neurovascular·Registered Apr 05, 2017 – Apr 05, 2022CancelledRegistration details
- Analysis ID
- c9c30d593c3837387221aa7ae2c03289
- License Form
- Ministry of Health Medical Device Import No. 029622
- Customs Code
- DHA05602962205
Company information
- Manufacturer
- Stryker Neurovascular
- Manufacturer Country
- Ireland
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- 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
- Apr 05, 2017
- Expiry Date
- Apr 05, 2022
- Cancellation Date
- May 23, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “Stryker” Surpass Streamline Flow Diverter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number c9c30d593c3837387221aa7ae2c03289 and manufactured by Stryker Neurovascular. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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