HydraSolve Console

GUDID 00857932006019

ANDREW TECHNOLOGIES LLC

Liposuction system

• Primary Device ID: 00857932006019
• NIH Device Record Key: c4d0a3e1-8075-4274-8505-df3668222d8c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HydraSolve Console
• Version Model Number: CON-03
• Company DUNS: 831171660
• Company Name: ANDREW TECHNOLOGIES LLC
• 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: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857932006019 [Primary]

FDA Product Code

• MUU: System, Suction, Lipoplasty

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-08-23
• Device Publish Date: 2016-09-22

Devices Manufactured by ANDREW TECHNOLOGIES LLC

• 00857932006019 - HydraSolve Console: 2018-08-23
• 00857932006019 - HydraSolve Console: 2018-08-23
• 00857932006026 - HydraSolve Sterile Treatment Ket: 2018-08-23