Identity
- Trade Name
- Surpass Streamline FDA UDI
- Generic Name
- Bare-metal intracranial vascular stent FDA UDI
- Device Name
- Flow Diverter FDA UDI
- Model / Reference
- M003SFD050200 FDA UDI
- Description
- Flow Diverter FDA UDI
Identifiers
- Catalog Number
- 124US FDA UDI
- Primary DI / UDI-DI
- 07613252648819 FDA UDI
- FDA Product Code
- OUT FDA UDI
- GMDN Term
- Bare-metal intracranial vascular stent FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Length — 20.0 Millimeter FDA UDILumen/Inner Diameter — 5.0 Millimeter FDA UDI
Category: Bare-metal intracranial vascular stent
Surpass Streamline by Stryker Corp. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI 858e6f63-b2c9-4a7d-948a-141fbbb3a194 37 fields · synced May 30, 2026