Taiwan FDA registration 262402d55752091bf710b461981370eb
"Stryker" Nu Maple micro conduction stent system
TW: “史賽克”紐偌楓微細傳導支架系統
Taiwan·Risk Class 3·Stryker Neurovascular·Registered Nov 02, 2009 – Nov 02, 2019CancelledRegistration details
- Analysis ID
- 262402d55752091bf710b461981370eb
- Customs Code
- DHA00602028807
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 Neuroscience
- Product Type (Level 2)
- K.5950 Artificial embolization device
- Import Information
- import
Dates and status
- Registration Date
- Nov 02, 2009
- Expiry Date
- Nov 02, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Stryker" Nu Maple micro conduction 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 262402d55752091bf710b461981370eb and manufactured by Stryker Neurovascular. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices