HydraSolve Sterile Treatment Ket

GUDID 00857932006026

ANDREW TECHNOLOGIES LLC

Liposuction system

• Primary Device ID: 00857932006026
• NIH Device Record Key: 7686c9f4-fd89-4d81-82a9-251745cdd15d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HydraSolve Sterile Treatment Ket
• Version Model Number: STK-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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857932006026 [Primary]

FDA Product Code

• MUU: System, Suction, Lipoplasty

Sterilization

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

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