oneNEST S 303-843508HS4FB-BIL

GUDID 00670482000692

oneNEST S 84" x 35'' is a non-powered foam surface

Umano Medical Inc

Foam bed mattress

• Primary Device ID: 00670482000692
• NIH Device Record Key: 3fb8716a-8733-475d-b6c1-a80e5eade633
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: oneNEST S
• Version Model Number: 303-843508HS4FB-BIL
• Catalog Number: 303-843508HS4FB-BIL
• Company DUNS: 249675476
• Company Name: Umano Medical Inc
• 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00670482000692 [Primary]
GS1	10670482000699 [Package]; Package: [1 Units]; In Commercial Distribution

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: 2023-05-08
• Device Publish Date: 2023-04-28

On-Brand Devices [oneNEST S]

• 00670482000692: oneNEST S 84" x 35'' is a non-powered foam surface
• 00670482000708: oneNEST S 80''x 35'' is a non-powered foam surface