| Primary Device ID | 10190302003407 |
| NIH Device Record Key | e7874c92-4af7-49cc-ad11-53e113cd5855 |
| Commercial Distribution Discontinuation | 2022-04-12 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Medium 199, Earle's |
| Version Model Number | 21180021 |
| Company DUNS | 229044524 |
| Company Name | LIFE TECHNOLOGIES LIMITED |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |