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

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
00816299012729 - PROS Wedge2024-04-24 PROS Wedge
00816299012750 - PROS Tail2024-04-24 Wedge with Tail
00816299010213 - HoverMatt T-Burg2022-10-04 Trendelenburg Patient Stabilization & Air Transfer Mattress
00816299011685 - HoverMatt SPU Plus HoverCover2022-10-04 34" HoverMatt Plus HoverCover Kit
00816299011708 - HoverMatt SPU Plus HoverCover2022-10-04 HoverMatt SPU Plus HoverCover
00816299010237 - HoverSling Repositiong Sling-TVA2021-11-08 39" Single Patient Use Repositioning HoverSling Breathable TVA

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