CureLight Medical Diode Laser Systems

GUDID 06976563460039

Wuhan PHOMED Technology Co., Ltd.

Musculoskeletal infrared phototherapy unit, non-wearable

• Primary Device ID: 06976563460039
• NIH Device Record Key: b52cbbb0-9a7a-4b4c-83de-7c1b41d83d64
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CureLight Medical Diode Laser Systems
• Version Model Number: CureLight F2-A30
• Company DUNS: 725228743
• Company Name: Wuhan PHOMED 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	06976563460039 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-11-24
• Device Publish Date: 2025-10-09

On-Brand Devices [CureLight Medical Diode Laser Systems]

• 06976563460107: CureLight S3-BF45
• 06976563460091: CureLight F4-ACDR45
• 06976563460084: CureLight F4-ABDR45
• 06976563460077: CureLight F4-ABCR45
• 06976563460060: CureLight F3-AB60
• 06976563460053: CureLight F3-AB30
• 06976563460046: CureLight F2-B30
• 06976563460039: CureLight F2-A30
• 06976563460022: CureLight F2-B15
• 06976563460015: CureLight F2-A15