Taiwan FDA registration 0c7d981001e2b5474dac8c296cb0e567
“Stryker” Neuroform Atlas Stent System
TW: “史賽克”紐偌楓艾特斯支架系統
Taiwan·Risk Class 3·MD·Stryker Neurovascular·Registered Jan 26, 2017 – Jan 26, 2027ActiveRegistration details
- Analysis ID
- 0c7d981001e2b5474dac8c296cb0e567
- License Form
- Ministry of Health Medical Device Import No. 029356
- Customs Code
- DHA05602935600
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
- Jan 26, 2017
- Expiry Date
- Jan 26, 2027
About this record
Access comprehensive regulatory information for “Stryker” Neuroform Atlas Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0c7d981001e2b5474dac8c296cb0e567 and manufactured by Stryker Neurovascular. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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