Maxicide Plus 1022865

GUDID 00304040003930

Sterilizing and Disinfecting Solution

HENRY SCHEIN, INC.

Glutaraldehyde device sterilant

• Primary Device ID: 00304040003930
• NIH Device Record Key: 7086d047-704b-4837-bcb5-e2ad8ae81f46
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Maxicide Plus
• Version Model Number: 1022865
• Catalog Number: 1022865
• Company DUNS: 012430880
• Company Name: HENRY SCHEIN, INC.
• Device Count: 1
• DM Exempt: true
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Dimensions

• Total Volume: 3.785 Liter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *STORE AT ROOM TEMPERATURE

Device Identifiers

Device Issuing Agency	Device ID
GS1	00304040003930 [Primary]

FDA Product Code

• MED: Sterilant, medical devices

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

On-Brand Devices [Maxicide Plus]

• 00304040003954: Sterilizing and Disinfecting Solution
• 00304040003930: Sterilizing and Disinfecting Solution