| Primary Device ID | 05407010125429 |
| NIH Device Record Key | f3af7a9d-0493-409b-ab25-50336af62433 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Production media supplement 2 - 500 ml |
| Version Model Number | BESP601SUP2F |
| Company DUNS | 370158847 |
| Company Name | Lonza Verviers |
| 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 |