Jetox JND-023

GUDID 07290014242913

TAV - TECH LTD

Pressure-regulated wound irrigation solution applicator, pneumatic

• Primary Device ID: 07290014242913
• NIH Device Record Key: 983994d4-0423-4ccd-b8a7-d738879193b8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Jetox
• Version Model Number: Jetox-ND23
• Catalog Number: JND-023
• Company DUNS: 531855211
• Company Name: TAV - TECH LTD
• Device Count: 1
• 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: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +97235360515
• Email: support@tav-tech.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290014242913 [Package]; Contains: 07290014242920; Package: [5 Units]; In Commercial Distribution
GS1	07290014242920 [Primary]

FDA Product Code

• FQH: Lavage, Jet

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-11-06
• Device Publish Date: 2019-10-29

On-Brand Devices [Jetox]

• 07290014242234: Jetox-ND
• 07290014242012: Jetox-HDC
• 07290014242913: Jetox-ND23
• 07290014242296: Jetox Tubing
• 07290014242265: Jetox tubing
• 07290014242302: Jetox tubing