FirstCare

GUDID 00817365020181

SELECT AIR OVERLAY SYSTEM (SASTDPUMP, SAOVERLAYMATT39, SAOVERLAYSHEET39)

MOXI ENTERPRISES, LLC

Alternating-pressure bed mattress overlay system

• Primary Device ID: 00817365020181
• NIH Device Record Key: ca553693-10c7-47f2-bc2e-79d7c720db13
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FirstCare
• Version Model Number: SAOVERLAYSYS39
• 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	00817365020181 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-09

On-Brand Devices [FirstCare]

• 00817365020181: SELECT AIR OVERLAY SYSTEM (SASTDPUMP, SAOVERLAYMATT39, SAOVERLAYSHEET39)
• 00817365020174: FIRST CARE MATTRESS OVERLAY SYSTEM French Canadian
• 00817365020167: FIRST CARE MATTRESS OVERLAY SYSTEM w/HYBPump
• 00817365020150: FIRST CARE MATTRESS OVERLAY SYSTEM w/STDPump