EVO

GUDID 06978181510219

Wuhan Qolight Technology Co., Ltd.

Musculoskeletal/physical therapy laser, professional

• Primary Device ID: 06978181510219
• NIH Device Record Key: 6392e661-51c9-4116-a787-1b1146b49ed3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EVO
• Version Model Number: EVO D30m
• Company DUNS: 714815435
• Company Name: Wuhan Qolight Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	06978181510219 [Primary]

FDA Product Code

• ILY: Lamp, Infrared, Therapeutic Heating

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: 2025-12-29
• Device Publish Date: 2025-12-19

On-Brand Devices [EVO]

• 06978181510233: EVO Q27m
• 06978181510226: EVO S9m
• 06978181510219: EVO D30m