961682

GUDID 10603295239802

UNIVERSAL REVISION FEMORAL BROACH HANDLE

DEPUY ORTHOPAEDICS, INC.

Surgical instrument handle, non-torque-limiting

• Primary Device ID: 10603295239802
• NIH Device Record Key: 0c085e0f-631f-4cab-b389-7bf445b06fae
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 96-1682
• Catalog Number: 961682
• Company DUNS: 080506581
• Company Name: DEPUY ORTHOPAEDICS, 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10603295239802 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-05-13
• Device Publish Date: 2018-09-24

Devices Manufactured by DEPUY ORTHOPAEDICS, INC.

• 10603295080121 - AML EXCEL: 2026-02-09 AML EXCEL FEMORAL/HUMERAL HEAD IMPACTOR
• 10603295082408 - DURALOC: 2026-02-09 DURALOC POLY IMPACTOR HANDLE
• 10603295083382 - SIGMA: 2026-02-09 SIGMA HP PARTIAL KNEE-UNI FEMORAL IMPACTOR
• 10603295084075 - SIGMA: 2026-02-09 SIGMA HP PARTIAL KNEE-TROCHLEA IMPACTOR
• 10603295088042 - GLOBAL FX: 2026-02-09 GLOBAL FX HEAD IMPACTION STAND
• 10603295090540 - GLOBAL AP: 2026-02-09 GLOBAL AP TAPER IMPACTOR
• 10603295090687 - GLOBAL AP: 2026-02-09 GLOBAL AP HEAD IMPACTOR
• 10603295094005 - NA: 2026-02-09 M.B.T. TRAY IMPACTOR