CORAIL/ TRI-LOCK 299964877

GUDID 10603295552222

CORAIL/TRI-LOCK MAKE TO ORDER 30-DEG STEM INSERTER

DEPUY ORTHOPAEDICS, INC.

Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable

• Primary Device ID: 10603295552222
• NIH Device Record Key: 6e71099c-830b-452d-a709-91426459cf3d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CORAIL/ TRI-LOCK
• Version Model Number: 2999-64-877
• Catalog Number: 299964877
• 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
• 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	10603295552222 [Primary]

FDA Product Code

• HWR: DRIVER, PROSTHESIS

Sterilization

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

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

[10603295552222]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-03-18
• Device Publish Date: 2024-03-08

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