XERF

GUDID 08809447658131

Lutronic Corporation

Radio-frequency skin/body contouring system

• Primary Device ID: 08809447658131
• NIH Device Record Key: 15558efc-927d-4d28-8301-315681f69b2b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: XERF
• Version Model Number: XERF EFFECTOR 60(900)
• Company DUNS: 688282516
• Company Name: Lutronic Corporation
• 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: 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	08809447657752 [Primary]
GS1	08809447657875 [Package]; Package: box [10 Units]; In Commercial Distribution
GS1	08809447658131 [Package]; Contains: 08809447657752; Package: box [1 Units]; In Commercial Distribution

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: 2025-09-29
• Device Publish Date: 2025-09-19

On-Brand Devices [XERF]

• 08809447657981: XERF
• 08809447658131: XERF EFFECTOR 60(900)