Cubby Beds

GUDID 00850043155072

Sensory Medical, Inc.

Bedside monitor remote-viewing software, non-physiological parameter

• Primary Device ID: 00850043155072
• NIH Device Record Key: b1aa022d-1388-4cfc-97da-897e1843f845
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cubby Beds
• Version Model Number: Dream Hub
• Company DUNS: 080980318
• Company Name: Sensory Medical, 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850043155072 [Primary]

FDA Product Code

• KMI: Monitor, Bed Patient

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: 2026-03-24
• Device Publish Date: 2026-03-16

On-Brand Devices [Cubby Beds]

• 00860007550263: Technology Hub Integrated system with camera, light, sensors, & speaker
• 00860007550249: Cubby Enclosed Bed Canopy System
• 00850043155072: Dream Hub