Fusion DF

GUDID 00817365021156

FUSION 42x80x8 Mattress with Dry Floatation Insert

MOXI ENTERPRISES, LLC

Orthopaedic bed mattress

• Primary Device ID: 00817365021156
• NIH Device Record Key: a05a801e-1c19-41e7-8761-87f3eed21bce
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fusion DF
• Version Model Number: FUSXL4280DF
• Company DUNS: 958807575
• Company Name: MOXI ENTERPRISES, LLC
• 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817365021156 [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: 2018-07-26
• Device Publish Date: 2018-06-25

On-Brand Devices [Fusion DF]

• 00817365021156: FUSION 42x80x8 Mattress with Dry Floatation Insert
• 00817365021676: FUSION 42x80x8 Mattress with Dry Floatation Insert