| Primary Device ID | 05407010125931 |
| NIH Device Record Key | 5eab59c9-8999-4af8-9a99-8d72776c77c0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IMDM Powder w/o HEPES, PR L-Glut, 1000L |
| Version Model Number | BE15-408K |
| Catalog Number | BE15-408K |
| 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 |