FusionXC

GUDID 00817365020372

FUSION XC SYSTEM, CUSTOM SIZE

MOXI ENTERPRISES, LLC

Orthopaedic bed mattress Orthopaedic bed mattress Orthopaedic bed mattress

• Primary Device ID: 00817365020372
• NIH Device Record Key: 4fa2704a-3154-4ebd-b499-26e3e36c2af8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FusionXC
• Version Model Number: FUSXCCUST
• 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	00817365020372 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-11

On-Brand Devices [FusionXC]

• 00817365021171: FUSION XC SYSTEM 39 x 80
• 00817365020402: MEDLINE FUSION PLUS MATTRESS W/VISCO HEEL SECTION, 80"
• 00817365020396: MEDLINE FUSION PLUS MATTRESS W/VISCO HEEL SECTION, 84"
• 00817365020389: MEDLINE FUSION PLUS MATTRESS W/VISCO HEEL SECTION, 80"
• 00817365020372: FUSION XC SYSTEM, CUSTOM SIZE
• 00817365020365: FUSION XC SYSTEM 84"
• 00817365020358: FUSION XC SYSTEM 80" W/VISCO HEEL & 1" VISCO TOP
• 00817365020341: FUSION XC SYSTEM 80"
• 00817365020334: FUSION XC SYSTEM 36" x 77"