| Primary Device ID | 00817463026825 |
| NIH Device Record Key | d41eb367-4d60-493d-929f-30495fa10feb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Physical Therapy Series |
| Version Model Number | PT250 Table |
| Company DUNS | 130256837 |
| Company Name | OAKWORKS, INC. |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817463026825 [Primary] |
| LGX | Table, Examination, Medical, 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 | 2023-08-17 |
| Device Publish Date | 2023-08-09 |
| 00817463026771 | PT150 Table 2 Section Top; 31" Width; 240V Electric PXSLA7311775MGTTZZEUPT |
| 00817463026764 | 2 Section Top; 29" Width; 240V Electric PXSLA7291775MGTTZZEUPT |
| 00817463026757 | 2 Section Top; 27" Width; 240V Electric PXSLA7271775MGTTZZEUPT |
| 00817463026702 | 1 Section Top; 29" Width; 240V Electric PXSLFT291873MGTTZZPTEU |
| 00817463026832 | 2 Section Top; 31" Width; 240V Electric PXSLA5311773MGTTZZEUPT |
| 00817463026825 | PT250 Table 2 Section Top; 29" Width; 240V Electric PXSLA5291773MGTTZZEUPT |
| 00817463026818 | PT250 Table 2 Section Top; 27" Width; 240V Electric PXSLA5271773MGTTZZEUPT |
| 00817463026696 | PT100 Table 1 Section Top; 27" Width; 240V Electric PXSLFT271873MGTTZZPTEU |
| 00817463026719 | PT100 Table 1 Section Top; 31" Width; 240V Electric |