NeoBar Large N713

GUDID 00812594011108

ET Tube Holder (Qty. 5)

NEOTECH PRODUCTS, INC.

Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Wearable percutaneous catheter/tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder

• Primary Device ID: 00812594011108
• NIH Device Record Key: 9f3b58bd-a1ac-463b-9dcb-0e209edb8985
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NeoBar Large
• Version Model Number: 10812594011105
• Catalog Number: N713
• Company DUNS: 198013435
• Company Name: NEOTECH PRODUCTS, INC.
• Device Count: 5
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812594011108 [Unit of Use]
GS1	10812594011105 [Primary]

FDA Product Code

• CBH: Device, Fixation, Tracheal Tube

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: 2021-06-10
• Device Publish Date: 2021-06-02

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