| Primary Device ID | 00855085005910 |
| NIH Device Record Key | 501ef610-2f6d-4084-b425-b3ca5da823ff |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Prime Medical LLC |
| Version Model Number | PrimePadPlus-K4 |
| Catalog Number | PrimePadPlus-K4 |
| Company DUNS | 078682939 |
| Company Name | Prime Medical LLC |
| 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 | 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 | true |