FDA UDI In Commercial Distribution 🇺🇸 United States

Surpass Elite

DI: 07613327583168 · Model: FDSE52512 · Stryker Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Surpass Elite
Primary DI
07613327583168
Version / Model
FDSE52512
Catalog Number
FDSE52512
Company Name
Stryker Corporation
Labeler DUNS
042405446
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-19
Public Version
3
Public Version Date
2026-03-30
Public Version Status
Update
Public Device Record Key
5deb3783-ae1a-4a71-9755-f2768fd5db7c

Device Description

Flow Diverter System

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OUT Intracranial aneurysm flow diverter

GMDN Terms

Code Name
46352 Bare-metal intracranial vascular stent

Identifiers

Type ID
Primary 07613327583168

Customer Contacts

Device Sizes

Type Value Unit Text
Length 12.0 Millimeter
Lumen/Inner Diameter 5.25 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in cool, dry, dark place.