| Primary Device ID | 00840075404194 |
| NIH Device Record Key | 98d4b559-f55a-4898-b63c-85bf095b08ae |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Formulation Buffer (pH 7.40 + 0.20) |
| Version Model Number | 04-1250Q (00307661) |
| Catalog Number | 04-1250Q (00307661) |
| Company DUNS | 609095955 |
| Company Name | Lonza Walkersville, 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 | false |
| Manufacturing Date | false |
| 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 |