| 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 |