217830136

GUDID 10603295094128

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

DEPUY ORTHOPAEDICS, INC.

Orthopaedic prosthesis implantation positioning instrument, reusable

• Primary Device ID: 10603295094128
• NIH Device Record Key: a258c634-d316-4ebf-b4e3-5ecc022fa313
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 2178-30-136
• Catalog Number: 217830136
• 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	10603295094128 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

Moist Heat or Steam Sterilization

[10603295094128]

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.

• 10603295094081 - NA: 2025-01-10 M.B.T. EVALUATION BULLET W/PEGS SIZE 1-3
• 10603295094098 - NA: 2025-01-10 M.B.T. EVALUATION BULLET W/PEGS SIZE 4-7
• 10603295094111 - NA: 2025-01-10 M.B.T. EVALUATION BULLET W/O PEGS SIZE 1-3
• 10603295094128 - NA: 2025-01-10M.B.T. EVALUATION BULLET W/O PEGS SIZE 4-7
• 10603295094128 - NA: 2025-01-10 M.B.T. EVALUATION BULLET W/O PEGS SIZE 4-7
• 10603295215738 - P.F.C.: 2025-01-10 P.F.C. MODULAR PLUS HEMI WEDGE TRIAL SZ 2 10 DEG
• 10603295215745 - P.F.C.: 2025-01-10 P.F.C. MODULAR PLUS HEMI WEDGE TRIAL SZ 2 20 DEG
• 10603295215776 - P.F.C.: 2025-01-10 P.F.C. MODULAR PLUS FULL WEDGE TRIAL SZ 2 10 DEG
• 10603295215783 - P.F.C.: 2025-01-10 P.F.C. MODULAR PLUS FULL WEDGE TRIAL SZ 2 15 DEG