Surgi-Max® Ultra

GUDID 00846338001643

ELLIQUENCE, LLC

Electrosurgical system

• Primary Device ID: 00846338001643
• NIH Device Record Key: 04b37199-688c-40ba-9e76-1cf0c8c873bd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Surgi-Max® Ultra
• Version Model Number: IEC6-SU120
• Company DUNS: 019872358
• Company Name: ELLIQUENCE, 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00846338001643 [Primary]

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2018-08-27
• Device Publish Date: 2018-07-26

On-Brand Devices [Surgi-Max® Ultra]

• 00846338001643: IEC6-SU120
• 00846338001438: IEC6-SU170