| Primary Device ID | 00817136023175 |
| NIH Device Record Key | f21e4dec-ee62-45c3-a410-1d9dbcd32b12 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 5510 7L SYRINGE |
| Version Model Number | 5510 |
| Catalog Number | CR1311 |
| 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 | false |
| Serial Number | true |
| 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 |