Painaway U800-305

GUDID 00852556007282

Multi Radiance Medical

Musculoskeletal infrared phototherapy unit, non-wearable

• Primary Device ID: 00852556007282
• NIH Device Record Key: c30eedba-e33b-4277-b63b-786649b70319
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Painaway
• Version Model Number: PainAway Homecare
• Catalog Number: U800-305
• Company DUNS: 826320694
• Company Name: Multi Radiance Medical
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00852556007282 [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: 2018-12-03
• Device Publish Date: 2018-11-01

On-Brand Devices [Painaway]

• 00852556007282: PainAway Homecare
• 00852556007091: PainAway PostOp Laser
• 00852556007299: PainAway
• 00852556007343: PainAway Home Care
• 00852556007336: PainAway