Surpass Elite Flow Diverter System (UDI P170024)
Manufactured by Stryker Neurovascular
Device Regulatory Overview
The Surpass Elite Flow Diverter System (Model/Catalog Number: Unspecified) is a medical device manufactured by Stryker Neurovascular. This product is indexed under FDA Product Code / Category Classification OUT within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- OUT
- Device Name
- Intracranial aneurysm flow diverter
- Database Sync Date
- 2026-08-09 10:04:45
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Surpass Elite Flow Diverter System?
The registered manufacturer of record for Surpass Elite Flow Diverter System is Stryker Neurovascular.
What is the Primary UDI-DI identifier for Surpass Elite Flow Diverter System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P170024.
What classification code is assigned to this device?
This device is registered under product classification code OUT.
Similar Classification Devices (OUT)
Other Devices by Stryker Neurovascular
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