AirLife™ 5104RDVX

GUDID 50190752146165

AirLife™ flow-inflating tail-end valve transport circuit

VYAIRE MEDICAL, INC.

Pulmonary resuscitator, manual, single-use

• Primary Device ID: 50190752146165
• NIH Device Record Key: cb519855-88df-4c8a-8082-8d58b5606872
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AirLife™
• Version Model Number: 5104RDVX
• Catalog Number: 5104RDVX
• Company DUNS: 080456871
• Company Name: VYAIRE MEDICAL, 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: 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: +1(833)327-3284
• Email: customersupport@vyaire.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10190752146167 [Primary]
GS1	50190752146165 [Package]; Contains: 10190752146167; Package: Case [20 Units]; In Commercial Distribution

FDA Product Code

• BTM: Ventilator, emergency, manual (resuscitator)

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: 2020-01-23
• Device Publish Date: 2020-01-15

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