Therarest

GUDID 05059441268512

Therarest, - Reactive Mattress Replacement

Arjohuntleigh AB

Foam-filled bed mattress overlay

• Primary Device ID: 05059441268512
• NIH Device Record Key: 65ec32dd-cd83-4254-9c50-606b02120820
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Therarest
• Version Model Number: TRMRLNB35084CHG
• Company DUNS: 355804758
• Company Name: Arjohuntleigh AB
• 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: false
• 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	05059441268512 [Primary]

FDA Product Code

• IKY: Mattress, Flotation Therapy, Non-Powered

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: 2022-08-08
• Device Publish Date: 2022-07-30

On-Brand Devices [Therarest]

• 05059441268512: Therarest, - Reactive Mattress Replacement
• 05059441268505: Therarest, - Reactive Mattress Replacement
• 05059441268499: Therarest VE, - Reactive Mattress Replacement
• 05059441268482: Therarest, - Reactive Mattress Replacement
• 05059441268475: Therarest, - Reactive Mattress Replacement
• 05056341697718: Therarest VE, - Reactive Mattress Replacement
• 05056341697695: Therarest, - Reactive Mattress Replacement
• 05059441203476: Therarest - Reactive Mattress Replacement Perimeter Plus 80 x 35 x 7 inches