3M™ Attest™ 1492VS

GUDID 50707387791914

3M™ Attest™ Super Rapid Readout Biological Indicator 1492VS, for Steam Sterilization, 50 Each/Carton, 2 Cartons/Case

3M COMPANY

Biological sterilization indicator

• Primary Device ID: 50707387791914
• NIH Device Record Key: 9e0f4136-42cf-4126-bb10-1af6a61e1db8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3M™ Attest™
• Version Model Number: 1492VS
• Catalog Number: 1492VS
• Company DUNS: 830016148
• Company Name: 3M COMPANY
• Device Count: 50
• 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: true
• 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

Customer Support Contacts

• Phone: 1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: 1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: 1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: 1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: 1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: 1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: 1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: 1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: 1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: 1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: 1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: 1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: 1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00707387762964 [Unit of Use]
GS1	30707387791910 [Primary]
GS1	50707387791914 [Package]; Contains: 30707387791910; Package: [2 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173437

FDA Product Code

• FRC: Indicator, Biological Sterilization Process

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: 2020-07-20
• Device Publish Date: 2020-07-10

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