Fullerton Manufacturing Limited

GUDID 08936235650043

FULLERTON MANUFACTURING LIMITED

Patient lifting system hammock sling

• Primary Device ID: 08936235650043
• NIH Device Record Key: e028f91b-c742-4112-af8e-99dce35afbed
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fullerton Manufacturing Limited
• Version Model Number: 1
• Company DUNS: 673129590
• Company Name: FULLERTON MANUFACTURING 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: true
• Lot Batch: true
• Serial Number: false
• 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	08936235650043 [Primary]

FDA Product Code

• FMR: Device, Transfer, Patient, Manual

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: 2025-07-10
• Device Publish Date: 2025-07-02

On-Brand Devices [Fullerton Manufacturing Limited]

• 08936235650012: 1
• 08936235650050: 1
• 08936235650043: 1
• 08936235650036: 1
• 08936235650029: 1
• 08936235650005: 1