Maxima Posterior 2283533

GUDID 10304040000820

Maxima Posterior

HENRY SCHEIN, INC.

Resin artificial teeth

• Primary Device ID: 10304040000820
• NIH Device Record Key: f1b4cc22-3367-4354-90eb-d92cce40f4c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Maxima Posterior
• Version Model Number: 2283533
• Catalog Number: 2283533
• Company DUNS: 012430880
• Company Name: HENRY SCHEIN, INC.
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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

Operating and Storage Conditions

• Storage Environment Temperature: Between 2 Degrees Celsius and 23 Degrees Celsius
• Storage Environment Temperature: Between 2 Degrees Celsius and 23 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00304040000823 [Primary]
GS1	10304040000820 [Package]; Contains: 00304040000823; Package: BOX [20 Units]; In Commercial Distribution

FDA Product Code

• ELM: Denture, plastic, teeth

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

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• 00304040192375 - Henry Schein: 2025-06-25 LOOP RECORDER PACK
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• 00304040192177 - Henry Schein: 2025-05-26 Pack Pain F/ Bradenton Surgical Center
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