| Primary Device ID | 05055272719674 |
| NIH Device Record Key | 9d8c23d6-170e-46b1-9d0d-3629cab2de28 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 532nm LIO |
| Version Model Number | 1205-P-2130 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05055272719674 [Primary] |
| HQF | Laser, Ophthalmic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-07-28 |
| Device Publish Date | 2021-07-20 |
| 05055272719674 - 532nm LIO | 2021-07-28 |
| 05055272719674 - 532nm LIO | 2021-07-28 |
| 05055272720328 - 514/810nm LIO | 2021-07-28 |
| 05055272720380 - 577nm LIO | 2021-07-28 |
| 05055272719926 - 3.6V PROFESSIONAL OPHTH IN CASE | 2020-03-06 |
| 05055272719933 - 3.6V SPECIALIST OPHTH IN CASE | 2020-03-06 |
| 05055272719940 - 3.6V PROFESSIONAL STREAK RETINOSCOPE IN CASE | 2020-03-06 |
| 05055272719957 - 3.6V PROFESSIONAL STREAK LED RETINOSCOPE IN CASE | 2020-03-06 |
| 05055272719964 - US PROFESSIONAL LED STUDENT KIT-SLIM | 2020-03-06 |