Cosyfit standard/Wide SR20259

GUDID 05060631840210

SAFESPACES (CORNHOLME) LIMITED

Safe environment patient enclosure

• Primary Device ID: 05060631840210
• NIH Device Record Key: 51639368-fbd3-4fce-9659-355f5c6c9aee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cosyfit standard/Wide
• Version Model Number: 183cm x 122cm - 91cm sides
• Catalog Number: SR20259
• Company DUNS: 349371893
• Company Name: SAFESPACES (CORNHOLME) LIMITED
• 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	05060631840210 [Primary]

FDA Product Code

• LLI: Bed, Therapeutic, Ac-Powered, Adjustable Home-Use

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: 2025-11-24
• Device Publish Date: 2025-11-12

On-Brand Devices [Cosyfit standard/Wide ]

• 50606318402410: 183cm x 122cm - 147cm sides
• 05060631840234: 183cm x 122cm - 122cm sides
• 05060631840227: 183cm x 122cm - 107cm sides
• 05060631840210: 183cm x 122cm - 91cm sides