Almore Aluminum Oxide

GUDID D248137730

Aluminum Oxide 4lb.

HAGER WORLDWIDE, INC.

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• Primary Device ID: D248137730
• NIH Device Record Key: 55f1ef0d-63b9-4e5b-8504-2ec94096cb7e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Almore Aluminum Oxide
• Version Model Number: 13773
• Company DUNS: 009277971
• Company Name: HAGER WORLDWIDE, 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D248137730 [Primary]

FDA Product Code

• EJR: AGENT, POLISHING, ABRASIVE, ORAL CAVITY

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-28
• Device Publish Date: 2024-05-20

On-Brand Devices [Almore Aluminum Oxide]

• D248137730: Aluminum Oxide 4lb.
• D248137720: Aluminum Oxide 1 lb.