| Primary Device ID | 05407010125221 |
| NIH Device Record Key | 7035ac08-043c-4ec4-ab42-b07bdac284e6 |
| Commercial Distribution Discontinuation | 2024-02-06 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | ProCHO5 powder supplement 2 Modified |
| Version Model Number | BESP441SUP2F175 |
| 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 |