LifeVac Home Kit

GUDID B712LVC3001

LIFEVAC, INC.

Airway emergency clearance/suction plunger

• Primary Device ID: B712LVC3001
• NIH Device Record Key: 9985145d-9ad5-4aa3-89c7-7336acf923c8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LifeVac Home Kit
• Version Model Number: LVC3001
• Company DUNS: 071298464
• Company Name: LIFEVAC, 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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
HIBCC	B712LVC3001 [Primary]

FDA Product Code

• GCX: Apparatus, Suction, Operating-Room, Wall Vacuum Powered

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: 2020-02-17
• Device Publish Date: 2020-02-07

Devices Manufactured by LIFEVAC, INC.

• B712LVC3002 - LifeVac EMS KIT: 2020-10-05
• B712LVC3003 - LifeVac School KIT: 2020-10-05
• B712LVC3004 - LifeVac Travel KIT: 2020-10-05
• B712LVC3001 - LifeVac Home Kit: 2020-02-17
• B712LVC3001 - LifeVac Home Kit: 2020-02-17