698342715

GUDID 10705034491202

MODIFIED INSTRUMENT GRAFT PUSHER

DEPUY SPINE, LLC

Orthopaedic graft inserter, reusable

• Primary Device ID: 10705034491202
• NIH Device Record Key: 44cbd5e3-55d2-45de-8f92-8118b2037379
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 698342715
• Catalog Number: 698342715
• Company DUNS: 107105876
• Company Name: DEPUY SPINE, LLC
• 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)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034491202 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

[10705034491202]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2024-08-20
• Device Publish Date: 2017-02-04

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• 10705034576473 - N/A: 2024-09-20 MODIFIED INSTRUMENT TAP
• 10705034576480 - N/A: 2024-09-20 MODIFIED INSTRUMENT DRIVER
• 10705034576534 - N/A: 2024-09-20 MODIFIED INSTRUMENT TAP
• 10705034576633 - N/A: 2024-09-19 MODIFIED INSTRUMENT OSTEOTOME
• 10705034576657 - N/A: 2024-09-19 MODIFIED INSTRUMENT DISTRACTOR LEG, SHORT
• 10705034576688 - N/A: 2024-09-19 MODIFIED INSTRUMENT ACDF SHIM