AGILON®

GUDID 04048844522865

metaphyseal component omarthrosis

implantcast GmbH

Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis Shoulder humeral body prosthesis

• Primary Device ID: 04048844522865
• NIH Device Record Key: e7d2eefd-9866-44ec-bd2f-8d52e80a5608
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AGILON®
• Version Model Number: 3821008300
• Company DUNS: 324369826
• Company Name: implantcast GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

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• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04048844522865 [Primary]

FDA Product Code

• HSD: Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-02-29
• Device Publish Date: 2024-02-21

On-Brand Devices [AGILON®]

• 04048844620103: osteotomy guide 145°
• 04048844522933: humeral cutting block 145°
• 04048844522926: trial metaphyseal component omarthrosis 145°
• 04048844522919: trial metaphyseal component omarthrosis 145°
• 04048844522902: trial metaphyseal component trauma 145°
• 04048844522865: metaphyseal component omarthrosis
• 04048844522858: metaphyseal component omarthrosis incl. safety screw
• 04048844522841: metaphyseal component omarthrosis
• 04048844522834: metaphyseal component omarthrosis incl. safety screw
• 04048844522827: metaphyseal component trauma
• 04048844522810: metaphyseal component trauma incl. safety screw