VivaSight-SL TVT80110

GUDID 07290013745026

Oral/Nasal Cuffed visualization Endotracheal tube

E.T. VIEW LTD

Basic endotracheal tube, single-use

• Primary Device ID: 07290013745026
• NIH Device Record Key: bcddebdc-e59f-4c84-89d2-80a0c04735fe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VivaSight-SL
• Version Model Number: TVT80110
• Catalog Number: TVT80110
• Company DUNS: 534096359
• Company Name: E.T. VIEW LTD
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +972-722607060
• Email: medical@ETView.com

Device Dimensions

• Outer Diameter: 8 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290013745026 [Primary]
GS1	17290013745023 [Package]; Package: Carton [10 Units]; In Commercial Distribution
GS1	27290013745020 [Package]; Contains: 17290013745023; Package: Carton [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K152438

FDA Product Code

• BTR: Tube, Tracheal (W/Wo Connector)

Sterilization

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

[07290013745026]

Ethylene Oxide

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 [VivaSight-SL]

• 07290013745026: Oral/Nasal Cuffed visualization Endotracheal tube
• 27290013745013: Oral/Nasal Cuffed visualization Endotracheal tube
• 07290013745002: Oral/Nasal Cuffed visualization Endotracheal tube