| Primary Device ID | 05407010126686 |
| NIH Device Record Key | aa6b5415-85c2-48eb-a1bb-f44d60c6db3b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | STD DMEM/F-12woCaCl2,HEPwoL-Glu,PR1000L |
| Version Model Number | VPW-014K |
| Catalog Number | VPW-014K |
| 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 |