| Primary Device ID | 05060745556656 |
| NIH Device Record Key | 82ff5f5f-5ac0-436b-b9f1-2f673175b555 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Capsulorhexis Forceps, Utrata Round Handle, CS, GT |
| Version Model Number | 11-5014 |
| Company DUNS | 738288096 |
| Company Name | BLINK MEDICAL 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 | true |
| 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 |