JetPeel JTO-003

GUDID 07290014242357

TAV - TECH LTD

Liquid-jet skin surface treatment system applicator, single-use

• Primary Device ID: 07290014242357
• NIH Device Record Key: 97396814-2afd-47b5-9456-a131ee835330
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JetPeel
• Version Model Number: JetPeel Tubing
• Catalog Number: JTO-003
• 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	07290014242357 [Primary]

FDA Product Code

• GFE: Brush, Dermabrasion, Powered

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: 2019-10-24
• Device Publish Date: 2019-10-16

On-Brand Devices [JetPeel]

• 07290014242395: 110V Blue
• 07290014242357: JetPeel Tubing
• 07290014242005: BiPhasic HP
• 07290014242364: Prestige Plus HP
• 07290014242067: Blue Line Magic HP
• 07290014242074: BiPhasic HP
• 07290014242463: 110V Black
• 07290014242340: N23 HP
• 07290014242333: N05 HP
• 07290014242319: N01 HP