Primary Device ID | 00817956023256 |
NIH Device Record Key | 99b7e2e4-1aa2-4ee4-9d27-2574878450fd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Repositioning - Tollos |
Version Model Number | T017LXBE |
Company DUNS | 049181763 |
Company Name | 1073849 Ontario Limited |
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 | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Height | 22 Inch |
Width | 11 Inch |
Depth | 14 Inch |
Height | 22 Inch |
Width | 11 Inch |
Depth | 14 Inch |
Height | 22 Inch |
Width | 11 Inch |
Depth | 14 Inch |
Height | 22 Inch |
Width | 11 Inch |
Depth | 14 Inch |
Height | 22 Inch |
Width | 11 Inch |
Depth | 14 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817956023256 [Primary] |
FSA | Lift, Patient, Non-Ac-Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-02-09 |
Device Publish Date | 2023-02-01 |
00817956023256 | Reusable Repositioning sling XXL 1000lbs/454kg color-coded binding full-length reclining sling |
00817956022303 | Repositioning Sling - Bariatric - 10 Loop - Poly Material - Single Patient Use |
00817956022280 | Repositioning Sling - Standard - 10 Loop - Poly Material - Single Patient Use |