| Primary Device ID | 05055272718035 |
| NIH Device Record Key | 88c0a13f-d4f7-4a1f-813e-f1ef1cb9ae92 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Keeler Kapture Lite to View Plus Upgrade |
| Version Model Number | 3020-P-7046 |
| Company DUNS | 210164398 |
| Company Name | KEELER LIMITED |
| Device Count | 1 |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |