AGILON® XO screw

GUDID 04048844400712

implantcast GmbH

Shoulder prosthesis screw

• Primary Device ID: 04048844400712
• NIH Device Record Key: e7aa1fa4-723c-4790-b311-baaf334c0ac6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AGILON® XO screw
• Version Model Number: 38610030
• 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

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04048844400712 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-02-19
• Device Publish Date: 2020-11-18

On-Brand Devices [AGILON® XO screw ]

• 04048844400750: 38610040
• 04048844400743: 38610037
• 04048844400736: 38610035
• 04048844400729: 38610032
• 04048844400712: 38610030
• 04048844400705: 38610022