Q2 Roller Lateral Turning Device HTR-200-1Roller

GUDID 00816299011647

Q2Roller w/ 5 pack of chux

Hovertech International

Patient transfer system, manual
Primary Device ID00816299011647
NIH Device Record Key139ad5e1-8e7a-416f-94ed-211440dbc4c1
Commercial Distribution StatusIn Commercial Distribution
Brand NameQ2 Roller Lateral Turning Device
Version Model NumberHTR-200-1Roller
Catalog NumberHTR-200-1Roller
Company DUNS942139841
Company NameHovertech International
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com
Phone6106949600
Emailspavelko@hovermatt.com

Device Dimensions

Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch
Width44 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100816299011647 [Package]
Contains: 00816299011678
Package: box [5 Units]
In Commercial Distribution
GS100816299011678 [Primary]

FDA Product Code

FMRDevice, Transfer, Patient, Manual

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-09-05
Device Publish Date2024-08-28

Devices Manufactured by Hovertech International

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00816299013047 - HoverMatt PROS Air Sling2026-03-09 The HoverMatt® PROS™(Patient Repositioning Off-Loading System) Air Sling, is breathable and used to assist caregivers with pa
00816299012194 - Single Patient Use HoverMatt2026-02-24 50" Single Patient Use Air Transfer Mattress: Regard(ROI)
00816299013016 - HoverMatt PROS Air Sling2026-02-24 Air Sling is breathable and used to assist caregivers with patient positioning (including boosting and turning), vertical lifts,
00816299011647 - Q2 Roller Lateral Turning Device2024-09-05Q2Roller w/ 5 pack of chux
00816299011647 - Q2 Roller Lateral Turning Device2024-09-05 Q2Roller w/ 5 pack of chux
00816299011586 - Q2Roller® Lateral Turning Device2024-08-30 Q2Roller Lateral Turning Device

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