JetPeel JTP333VBK110

GUDID 07290014242463

110V Black

TAV - TECH LTD

Liquid-jet skin surface treatment system control unit

• Primary Device ID: 07290014242463
• NIH Device Record Key: d534ddd3-a6b9-4823-b43e-22b083e07f95
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JetPeel
• Version Model Number: JetPeel-3V
• Catalog Number: JTP333VBK110
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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	07290014242463 [Primary]

FDA Product Code

• GFE: Brush, Dermabrasion, Powered

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: 2019-11-06
• Device Publish Date: 2019-10-29

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• 07290014242319: N01 HP