| Primary Device ID | G5102959 |
| NIH Device Record Key | b0e01637-12a8-4764-a806-352d6c634ef8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BRILLIANCE |
| Version Model Number | 2959 |
| Company DUNS | 075058495 |
| Company Name | Light Sources, Inc. |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | G5102959 [Primary] |
| LEJ | Booth, Sun Tan |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-02-12 |
| Device Publish Date | 2025-02-04 |
| G51029540 | 2954 |
| G51022430 | 2243 |
| G510197701 | 1977 |
| G51014810 | 1481 |
| G51008240 | 0824 |
| G51026670 | 2667 |
| G51022480 | 2248 |
| G51019630 | 1963 |
| G51030440 | 3044 |
| G510295700 | 2957 |
| G51032380 | 3238 |
| G51030990 | 3099 |
| G51019750 | 1975 |
| G510196700 | 1967 |
| G51008620 | 0862 |
| G510295801 | 2958 |
| G51022460 | 2246 |
| G5103236 | 3236 |
| G51019730 | 1973 |
| G5103237 | 3237 |
| G5103235 | 3235 |
| G5103123 | 3123 |
| G5102959 | 2959 |
| G51019720 | 1972 |
| G51032470 | 3247 |
| G51029520 | 2952 |
| G51030960 | 3096 |
| G51029220 | 2922 |
| G51019740 | 1974 |
| G51032330 | 3233 |
| G51032320 | 3232 |