PPS Glide

GUDID 00860010693131

Regular

PATIENT POSITIONING SYSTEMS, LLC

Inflatable patient transfer sliding mattress, single-use

• Primary Device ID: 00860010693131
• NIH Device Record Key: d65c1402-7cde-4227-bbb4-496e5cdaee40
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PPS Glide
• Version Model Number: SPU Regular
• Company DUNS: 013007744
• Company Name: PATIENT POSITIONING SYSTEMS, LLC
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860010693131 [Primary]

FDA Product Code

• FRZ: Device, Patient Transfer, 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: 2025-01-21
• Device Publish Date: 2025-01-13

On-Brand Devices [PPS Glide]

• 00860010693131: Regular
• 00860010693100: Regular
• 00860010693155: SPU Bariatric
• 00860010693148: SPU Large
• 00860010693124: Reusable Bariatric
• 00860010693117: Reusable Large