| Primary Device ID | 06973494938002 |
| NIH Device Record Key | d6ae03a7-a393-4cb5-8974-1141a62561c6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Globalipl |
| Version Model Number | US800 |
| Company DUNS | 544936742 |
| Company Name | BEIJING GLOBALIPL DEVELOPMENT CO., 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |