Enhance RDX

GUDID 00817365021188

Alternating pressure mattress

MOXI ENTERPRISES, LLC

Low-air-loss bed

• Primary Device ID: 00817365021188
• NIH Device Record Key: 99dcb01b-eff8-4981-85d4-e6a180ee3ec8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Enhance RDX
• Version Model Number: FM-MOX0046
• 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817365021188 [Primary]

FDA Product Code

• FNM: Mattress, Air Flotation, Alternating Pressure

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: 2020-04-07
• Device Publish Date: 2020-03-30

On-Brand Devices [Enhance RDX]

• 00817365021195: Enhance RDX Control Unit
• 00817365021188: Alternating pressure mattress