| Primary Device ID | 00893398002035 |
| NIH Device Record Key | ebafe7d9-6bbb-4a15-97df-7cbd6991f02e |
| Commercial Distribution Discontinuation | 2023-01-01 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | DENVER SPLINT |
| Version Model Number | 10-4021-05KS |
| Company DUNS | 051437143 |
| Company Name | SHIPPERT MEDICAL TECHNOLOGIES, 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |