DigiFuse® Cannulated Intramedullary Fusion System DF2600

GUDID M269DF26001

Integra® DigiFuse® The DigiFuse driver shaft is used to create holes when inserted into a driver handle.

Ascension Orthopedics, Inc.

Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable

• Primary Device ID: M269DF26001
• NIH Device Record Key: c0012d51-52a1-4574-9f77-2f05e86a413f
• Commercial Distribution Discontinuation: 2026-12-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DigiFuse® Cannulated Intramedullary Fusion System
• Version Model Number: DF2600
• Catalog Number: DF2600
• Company DUNS: 942377524
• Company Name: Ascension Orthopedics, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10381780244431 [Primary]
HIBCC	M269DF26001 [Secondary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

[M269DF26001]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2023-02-22
• Device Publish Date: 2017-09-05

On-Brand Devices [DigiFuse® Cannulated Intramedullary Fusion System]

• M269DF26801: Integra® DigiFuse® The forceps are used for screw pickup in the Integra DigiFuse system.
• M269DT4500L1: Integra® DigiFuse® The DigiFuse Lid is the top part of the sterilization tray which locks onto
• M269DT45001: Integra® DigiFuse® The DigiFuse Instrument Sterilization Tray is designed to contain, secure,
• M269DT3500LID1: Integra® DigiFuse® The DigiFuse Lid is the top part of the tray which locks onto the base and
• M269DT35001: Integra® DigiFuse® The DigiFuse Instrument Sterilization Tray is designed to contain, secure,
• M269DF26101: Integra® DigiFuse® The DigiFuse driver shaft is used to create holes when inserted into a driv
• M269DF26001: Integra® DigiFuse® The DigiFuse driver shaft is used to create holes when inserted into a driv
• M269DF15001: Integra® DigiFuse® The ratchet handle is used in conjunction with the Integra DigiFuse system.
• M269DW25901: Integra® DigiFuse® The smooth guide wire is used as a guide for placement or insertion of a de