UNIVERSAL HIGH BACK MESH EXTRA LARGE M921533-XL

GUDID 05056387435978

SILVALEA LIMITED

General-purpose patient lifting system sling/harness

• Primary Device ID: 05056387435978
• NIH Device Record Key: cf2e1fc8-4cfb-451e-8607-4874bb6ed16d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UNIVERSAL HIGH BACK MESH EXTRA LARGE
• Version Model Number: M921533-XL
• Catalog Number: M921533-XL
• Company DUNS: 423632996
• Company Name: SILVALEA 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: 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	05056387435978 [Primary]

FDA Product Code

• INE: Sling, Overhead Suspension, Wheelchair

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: 2024-03-05
• Device Publish Date: 2024-02-26

On-Brand Devices [UNIVERSAL HIGH BACK MESH EXTRA LARGE]

• 05056387435978: M921533-XL
• 05056387405827: CCR400MXL