Safespace SR2013

GUDID 05060631840524

SAFESPACES (CORNHOLME) LIMITED

Safe environment patient enclosure

• Primary Device ID: 05060631840524
• NIH Device Record Key: abcd6d04-f991-4cee-8fc2-d5e34d415593
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Safespace
• Version Model Number: 200cm x 300cm x 204cm h
• Catalog Number: SR2013
• 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	05060631840524 [Primary]

FDA Product Code

• FNJ: Bed, Manual

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 [Safespace]

• 05060631840531: 250cm x 300cm x 204cm h
• 05060631840524: 200cm x 300cm x 204cm h