Soltive Gemini

GUDID 00810071230875

Laser Universal Footswitch

IPG Medical Corporation

General/multiple surgical solid-state laser system

• Primary Device ID: 00810071230875
• NIH Device Record Key: f25eab7b-a3f9-4361-9f17-b9a2a82df647
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Soltive Gemini
• Version Model Number: MD2300F-003682
• Company DUNS: 081504133
• Company Name: IPG Medical 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810071230875 [Primary]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

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: 2025-12-10
• Device Publish Date: 2025-12-02

On-Brand Devices [Soltive Gemini]

• 00810071230899: Soltive Gemini 60W Laser System
• 00810071230882: Soltive Gemini 60W Laser Console
• 00810071230875: Laser Universal Footswitch