Neo-Vent™

GUDID 10709078004664

Infant T-Piece Resuscitation Circuit w/ Infant Neonate Masks

WESTMED, INC.

Pulmonary resuscitator, manual, single-use

• Primary Device ID: 10709078004664
• NIH Device Record Key: eb8f7b21-acaf-492d-8815-bee4ec93a4c8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Neo-Vent™
• Version Model Number: 0419
• Company DUNS: 092673953
• Company Name: WESTMED, 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00709078004667 [Primary]
GS1	10709078004664 [Package]; Contains: 00709078004667; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K923618

FDA Product Code

• BYE: Attachment, Breathing, Positive End Expiratory Pressure

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: 2017-10-27

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