| Primary Device ID | 00861028000300 |
| NIH Device Record Key | f5e5d0da-a621-44b6-9311-4db9f71e04b5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Leeches USA |
| Version Model Number | LE2000 |
| Company DUNS | 603572942 |
| Company Name | LEECHES USA LTD |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | false |