| Primary Device ID | 05055272700894 |
| NIH Device Record Key | 28293b8f-9e12-4caf-a778-62fa81216fb9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 2.8V SPECIALIST OPHTH IN CASE |
| Version Model Number | 1132-P-1149 |
| 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 | true |
| Serial Number | false |
| 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 |