Quasar MD

GUDID 06975965180187

Ningbo Yimei Nikko-seiki Manufacture Co.,LTD

Red/infrared light phototherapy unit

• Primary Device ID: 06975965180187
• NIH Device Record Key: 354ff10a-4a86-4315-bc9f-ae19244cb4d0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Quasar MD
• Version Model Number: TN2425
• Company DUNS: 553152875
• Company Name: Ningbo Yimei Nikko-seiki Manufacture 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: true
• 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	06975965180187 [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: 2025-08-21
• Device Publish Date: 2025-08-13

Devices Manufactured by Ningbo Yimei Nikko-seiki Manufacture Co.,LTD

• 06975965180187 - Quasar MD: 2025-08-21
• 06975965180187 - Quasar MD: 2025-08-21
• 06975965182006 - SPORTSMAX: 2025-01-21
• 06975965182013 - SPORTSMAX: 2025-01-21
• 06975965182020 - SPORTSMAX: 2025-01-21