PowerLaser Basic 1600 Platinum

GUDID 57135920351647

Powermedic ApS

Musculoskeletal/physical therapy laser, home-use

• Primary Device ID: 57135920351647
• NIH Device Record Key: 96ae51e9-c8a3-4650-9561-31c1e8518713
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PowerLaser Basic 1600 Platinum
• Version Model Number: 35164
• Company DUNS: 305378978
• Company Name: Powermedic ApS
• 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: false
• 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	57135920351647 [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: 2023-06-21
• Device Publish Date: 2023-06-13

On-Brand Devices [PowerLaser Basic 1600 Platinum]

• 57135920351647: 35164
• 05713592351645: 35164