| Primary Device ID | 00817136023182 |
| NIH Device Record Key | 86983910-f1a2-4772-bab9-538b0b336a7a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 6005 NDGB |
| Version Model Number | 6005 |
| Catalog Number | CR1346 |
| 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 |