GigaLaser

GUDID 05713592022255

Powermedic ApS

Musculoskeletal/physical therapy laser, professional

• Primary Device ID: 05713592022255
• NIH Device Record Key: 7313d0a3-d899-4f49-b41c-53ffe1ebda91
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GigaLaser
• Version Model Number: 2225
• 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	05713592022255 [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: 4
• Public Version Date: 2019-05-07
• Device Publish Date: 2016-11-22

Devices Manufactured by Powermedic ApS

• 05713592301824 - PowerLaser Basic1800 Vet Cool Grey: 2024-04-03
• 05713592301831 - PowerLaser Basic1800 Vet Olive Green: 2024-04-03
• 05713592301848 - PowerLaser Basic1800 Vet Platinum: 2024-04-03
• 05713592400558 - PowerLaser Pro500 VET Red: 2023-10-24
• 05713592401555 - PowerLaser Pro1500 VET Red: 2023-10-24
• 05713592451215 - PowerLaser Pro1200 Black: 2023-10-24
• 05713592451253 - PowerLaser Pro1200 Red: 2023-10-24
• 05713592500104 - PowerLaser Pro1200 White: 2023-10-24