217830133

GUDID 10603295094098

M.B.T. EVALUATION BULLET W/PEGS SIZE 4-7

DEPUY ORTHOPAEDICS, INC.

Orthopaedic prosthesis implantation positioning instrument, reusable

• Primary Device ID: 10603295094098
• NIH Device Record Key: 5ed37473-3dac-4310-b259-d7a47812e3b3
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 2178-30-133
• Catalog Number: 217830133
• 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	10603295094098 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

[10603295094098]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-01-10
• Device Publish Date: 2018-09-24

Devices Manufactured by DEPUY ORTHOPAEDICS, INC.

• 10603295548997 - SIGMA: 2025-04-10 SIGMA MAKE TO ORDER HP 5 DEGREE TIBIAL CUTTING BLOCK RIGHT
• 10603295549031 - SIGMA: 2025-04-10 SIGMA MAKE TO ORDER HP 5 DEGREE TIBIAL CUTTING BLOCK LEFT
• 10603295552673 - ATTUNE: 2025-04-01 ATTUNE MAKE TO ORDER PATELLA MED DOME DRILL TRIAL 29mm
• 10603295552697 - ATTUNE: 2025-04-01 ATTUNE MAKE TO ORDER PATELLA MED DOME DRILL TRIAL 41mm
• 10603295552710 - ATTUNE: 2025-04-01 ATTUNE MAKE TO ORDER PATELLA MED DOME DRILL TRIAL 32mm
• 10603295552796 - ATTUNE: 2025-04-01 ATTUNE MAKE TO ORDER PATELLA MED DOME DRILL TRIAL 35mm
• 10603295552802 - ATTUNE: 2025-04-01 ATTUNE MAKE TO ORDER PATELLA MED DOME DRILL TRIAL 38mm
• 10603295555476 - ATTUNE: 2025-04-01 ATTUNE TM MAKE TO ORDER CLASSIC SLAP HAMMER ASSEMBLY