| Primary Device ID | 08800056263990 |
| NIH Device Record Key | ddb98a16-d9ca-4545-ad4f-b6d7ef85539e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Peridot Intervertebral body fusion system |
| Version Model Number | L362-4050 |
| Company DUNS | 694609156 |
| Company Name | GBS Commonwealth 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |