Arjo Loop Ambulatory Sling MLA5100-M

GUDID 05059441380467

Loop Ambulatory Sling - M

Arjohuntleigh AB

General-purpose patient lifting system sling/harness

• Primary Device ID: 05059441380467
• NIH Device Record Key: 938a0734-fc34-4d38-b9fb-c62e33bef227
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Arjo Loop Ambulatory Sling
• Version Model Number: MLA5100-M
• Catalog Number: MLA5100-M
• Company DUNS: 355804758
• Company Name: Arjohuntleigh AB
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	05059441380467 [Primary]

FDA Product Code

• FSA: Lift, Patient, Non-Ac-Powered

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: 2026-03-17
• Device Publish Date: 2026-03-09

On-Brand Devices [Arjo Loop Ambulatory Sling]

• 05059441380481: Loop Ambulatory Sling - XL
• 05059441380474: Loop Ambulatory Sling - L
• 05059441380467: Loop Ambulatory Sling - M
• 05059441380450: Loop Ambulatory Sling - S