Henry Schein Maxima 5700484

GUDID 00304040117422

Maxima Capsule Mixer

HENRY SCHEIN, INC.

Dental impression material mixer

• Primary Device ID: 00304040117422
• NIH Device Record Key: 27393508-46f1-4c77-9cee-e2975aa8b75c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Henry Schein Maxima
• Version Model Number: 5700484
• Catalog Number: 5700484
• Company DUNS: 012430880
• Company Name: HENRY SCHEIN, 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: false
• Serial Number: true
• Manufacturing Date: false
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00304040117422 [Primary]

FDA Product Code

• EFD: AMALGAMATOR, DENTAL, AC-POWERED

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: 2019-12-04
• Device Publish Date: 2019-11-26

On-Brand Devices [Henry Schein Maxima]

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