Maxima Turbo 5703362

GUDID 00304040169834

Maxima Turbo Class B Sterilizer

HENRY SCHEIN, INC.

Steam sterilizer

• Primary Device ID: 00304040169834
• NIH Device Record Key: 2241aa5c-a71e-45ab-b14f-ce102ed53101
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Maxima Turbo
• Version Model Number: 5703362
• Catalog Number: 5703362
• 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: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00304040169834 [Primary]

FDA Product Code

• FLE: Sterilizer, steam

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: 2024-07-03
• Device Publish Date: 2024-06-25

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