FDA UDI In Commercial Distribution 🇺🇸 United States

DigiFuse® Cannulated Intramedullary Fusion System

DI: 10381780244844 · Model: DW-2590 · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
DigiFuse® Cannulated Intramedullary Fusion System
Primary DI
10381780244844
Version / Model
DW-2590
Catalog Number
DW-2590
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-05
Public Version
6
Public Version Date
2024-09-11
Public Version Status
Update
Public Device Record Key
aa9dfb6a-bd13-41ae-8a4c-f6cabb2369e5
Distribution End Date
2026-12-31

Device Description

Integra® DigiFuse® The smooth guide wire is used as a guide for placement or insertion of a device.

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HXI PASSER, WIRE, ORTHOPEDIC

GMDN Terms

Code Name
46165 Orthopaedic guidewire, reusable

Identifiers

Type ID
Secondary M269DW25901
Primary 10381780244844

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 2.756 in L x .031 in dia