Accora FloorBed KWNSB-W-FL8-000US

GUDID 05056147701091

Alesso Wide, Four Section Profiling Bed

ACCORA LIMITED

Electrical assistive bed

• Primary Device ID: 05056147701091
• NIH Device Record Key: dae076af-4830-48ea-a62e-972cfcf9c9f6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Accora FloorBed
• Version Model Number: Alesso Wide
• Catalog Number: KWNSB-W-FL8-000US
• Company DUNS: 736558755
• Company Name: ACCORA LIMITED
• 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	05056147701091 [Primary]

FDA Product Code

• FNL: Bed, Ac-Powered Adjustable Hospital

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: 2024-10-03
• Device Publish Date: 2024-09-25

On-Brand Devices [Accora FloorBed]

• 05056147700063: FloorBed 1 Plus, 4 Section Profiling Bed
• 05056147700001: FloorBed 1, 4 Section Profiling Bed
• 05056147700209: FloorBed 6, 4 Section Profiling Bed
• 05056147701091: Alesso Wide, Four Section Profiling Bed
• 05056147701084: Alesso, Four Section Profiling Bed