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 |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com | |
Phone | 6106949600 |
spavelko@hovermatt.com |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00816299011586 [Primary] |
FMR | Device, Transfer, Patient, Manual |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-30 |
Device Publish Date | 2024-08-22 |
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 |
00816299012729 - PROS Wedge | 2024-04-24 PROS Wedge |
00816299012750 - PROS Tail | 2024-04-24 Wedge with Tail |
00816299010213 - HoverMatt T-Burg | 2022-10-04 Trendelenburg Patient Stabilization & Air Transfer Mattress |
00816299011685 - HoverMatt SPU Plus HoverCover | 2022-10-04 34" HoverMatt Plus HoverCover Kit |
00816299011708 - HoverMatt SPU Plus HoverCover | 2022-10-04 HoverMatt SPU Plus HoverCover |
00816299010237 - HoverSling Repositiong Sling-TVA | 2021-11-08 39" Single Patient Use Repositioning HoverSling Breathable TVA |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
Q2ROLLER 86609252 5082998 Live/Registered |
D.T. DAVIS ENTERPRISES, LTD. 2015-04-24 |