| Primary Device ID | 05032384005765 |
| NIH Device Record Key | 53cb2bf4-6fb0-4344-bc2b-f8c3649f1638 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | CT0031B |
| Company DUNS | 365355452 |
| Company Name | OXOID LIMITED |
| Device Count | 5 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | false |
| OTC Over-The-Counter | false |