| Primary Device ID | 00874750008087 |
| NIH Device Record Key | 1c4f0bb1-8658-4a4d-98b0-bdda47e27cb2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 6030 NDGB |
| Version Model Number | 6030 |
| Catalog Number | 112113 |
| Company DUNS | 007131725 |
| Company Name | HANS RUDOLPH, 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 | false |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |