PPS Air Blower

GUDID 00860010693179

PATIENT POSITIONING SYSTEMS, LLC

Alternating-pressure inflator

• Primary Device ID: 00860010693179
• NIH Device Record Key: 04587f7c-ed9c-469b-b80a-836adcb1689c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PPS Air Blower
• Version Model Number: US Version
• 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: false
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860010693179 [Primary]

FDA Product Code

• CCX: Support, Patient Position

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: 2025-01-22
• Device Publish Date: 2025-01-14

Devices Manufactured by PATIENT POSITIONING SYSTEMS, LLC

• 00860010693117 - PPS Glide: 2025-01-22
• 00860010693124 - PPS Glide: 2025-01-22
• 00860010693148 - PPS Glide: 2025-01-22
• 00860010693155 - PPS Glide: 2025-01-22
• 00860010693179 - PPS Air Blower: 2025-01-22
• 00860010693179 - PPS Air Blower: 2025-01-22
• 00860010693100 - PPS Glide: 2025-01-21 Regular
• 00860010693131 - PPS Glide: 2025-01-21 Regular