PRIUS

GUDID 04717677480122

AIR MATTRESS

CAREMED SUPPLY INC.

Alternating-pressure bed mattress overlay system

• Primary Device ID: 04717677480122
• NIH Device Record Key: 9b4fe27f-95cc-40af-afc5-a708367200f1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRIUS
• Version Model Number: FM-PHR0037
• Company DUNS: 657602459
• Company Name: CAREMED SUPPLY INC.
• 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: 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	04717677480122 [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: 2016-11-25

On-Brand Devices [PRIUS]

• 04717677480184: AIR MATTRESS
• 04717677480177: AIR MATTRESS
• 04717677480160: AIR MATRESS
• 04717677480153: AIR MATTRESS
• 04717677480146: AIR MATTRESS
• 04717677480139: AIR MATTRESS
• 04717677480122: AIR MATTRESS
• 04717677480115: AIR MATTRESS
• 04717677480108: AIR MATTRESS
• 04717677480092: AIR MATTRESS
• 04717677480085: AIR MATTRESS
• 04717677480078: AIR MATTRESS
• 04717677480061: AIR MATTRESS
• 04717677480054: AIR MATTRESS
• 24717677480041: AIR MATTRESS CONTROLLER
• 24717677480034: AIR MATTRESS CONTROLLER
• 44717677480021: Air Mattress Controller