ResQUp

GUDID 00860003643105

Self-Recovery device to assist a fallen person moving themselves to a seated position after a non-injurious fall. Color: Midnight

Safe Patient Solutions, L.L.C.

Mobile patient lifting system, manual

• Primary Device ID: 00860003643105
• NIH Device Record Key: c5f597de-299b-4a25-a7bd-9207f8e5fbd4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ResQUp
• Version Model Number: Midnight
• Company DUNS: 017840548
• Company Name: Safe Patient Solutions, L.L.C.
• 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: false
• Manufacturing Date: false
• 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	00860003643105 [Primary]

FDA Product Code

• IKX: Aid, Transfer

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: 2021-12-17
• Device Publish Date: 2021-12-09

On-Brand Devices [ResQUp]

• 00860003643129: Self-Recovery device to assist a fallen person moving themselves to a seated position after a no
• 00860003643112: Self-Recovery device to assist a fallen person moving themselves to a seated position after a no
• 00860003643105: Self-Recovery device to assist a fallen person moving themselves to a seated position after a no
• 00860003643136: Self-Recovery device to assist a fallen person moving themselves to a seated position after a no