Avance 7703014

GUDID 07323190130894

TALLEY GROUP LIMITED

Negative-pressure wound therapy system, battery-powered, reusable

• Primary Device ID: 07323190130894
• NIH Device Record Key: 836802fb-f093-4ec7-bdda-6d591b1b10f6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Avance
• Version Model Number: 7703014-00
• Catalog Number: 7703014
• Company DUNS: 216861104
• Company Name: TALLEY GROUP LIMITED
• 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: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07323190130870 [Primary]
GS1	07323190130894 [Package]; Contains: 07323190130870; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• OMP: negative pressure wound therapy Powered suction pump

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

On-Brand Devices [Avance]

• 07323190130948: 7703006-00
• 07323190130894: 7703014-00
• 07323190130856: 7703013-00
• 07323190130733: 7703000-00
• 07323190130610: 7702013-00
• 07323190130535: 7702003-00
• 07323190130412: 7702006-00
• 07323190130375: 7702000-00