ViroMax 156200

GUDID 00817081020304

Filter, Disposable,Viral/ Bacterial - ViroMax

A-M SYSTEMS, LLC

Pulmonary function testing filter/mouthpiece Pulmonary function testing filter/mouthpiece Pulmonary function testing filter/mouthpiece

• Primary Device ID: 00817081020304
• NIH Device Record Key: 506cad9d-b39e-4f85-973d-c9efd91316a4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ViroMax
• Version Model Number: ViroMax - 156200
• Catalog Number: 156200
• Company DUNS: 020275145
• Company Name: A-M SYSTEMS, LLC
• 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: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 3606838300
• Email: sales@a-msystems.com
• Phone: 3606838300
• Email: sales@a-msystems.com
• Phone: 3606838300
• Email: sales@a-msystems.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817081020298 [Primary]
GS1	00817081020304 [Package]; Contains: 00817081020298; Package: [50 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K063526

FDA Product Code

• CAH: Filter, Bacterial, Breathing-Circuit

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

On-Brand Devices [ViroMax]

• 00817081020304: Filter, Disposable,Viral/ Bacterial - ViroMax
• 00817081027280: Filter, Disposable,Viral/ Bacterial - ViroMax