Q2Roller® Lateral Turning Device Q2R-100-1

GUDID 00816299011586

Q2Roller Lateral Turning Device

Hovertech International

Patient transfer system, manual

• Primary Device ID: 00816299011586
• NIH Device Record Key: 9e878ec8-5a24-4b91-923a-ac40f1f731ad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Q2Roller® Lateral Turning Device
• Version Model Number: Q2R-100-1
• Catalog Number: Q2R-100-1
• Company DUNS: 942139841
• Company Name: Hovertech International
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com
• Phone: 6106949600
• Email: spavelko@hovermatt.com

Device Dimensions

• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch
• Width: 44 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816299011586 [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: 2024-08-30
• Device Publish Date: 2024-08-22

Devices Manufactured by Hovertech International

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• 00816299012996 - HoverMatt PROS Air: 2026-03-09 The HoverMatt® PROS™ (Patient Repositioning Off-Loading System) Air, is breathable and used to assist caregivers with patient
• 00816299013047 - HoverMatt PROS Air Sling: 2026-03-09 The HoverMatt® PROS™(Patient Repositioning Off-Loading System) Air Sling, is breathable and used to assist caregivers with pa
• 00816299012194 - Single Patient Use HoverMatt: 2026-02-24 50" Single Patient Use Air Transfer Mattress: Regard(ROI)
• 00816299013016 - HoverMatt PROS Air Sling: 2026-02-24 Air Sling is breathable and used to assist caregivers with patient positioning (including boosting and turning), vertical lifts,
• 00816299011647 - Q2 Roller Lateral Turning Device: 2024-09-05 Q2Roller w/ 5 pack of chux
• 00816299011586 - Q2Roller® Lateral Turning Device: 2024-08-30Q2Roller Lateral Turning Device
• 00816299011586 - Q2Roller® Lateral Turning Device: 2024-08-30 Q2Roller Lateral Turning Device