| Primary Device ID | G5102578 |
| NIH Device Record Key | f067b6e5-0ff6-4f23-a9da-f725fc1ada25 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UV POWER |
| Version Model Number | 2578 |
| 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 | G5102578 [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 | 2024-11-25 |
| Device Publish Date | 2024-11-15 |
| G51024590 | 2459 |
| G51024090 | 2409 |
| G5102578 | FR2000T12/VHO/BP/8.5/230 200W |
| G51017960 | 1796 |
| G51024580 | 2458 |
| G51024570 | 2457 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() UV POWER 78504180 3221304 Dead/Cancelled |
UV-POWER LICHT GMBH 2004-10-22 |
![]() UV POWER 76269502 not registered Dead/Abandoned |
UV POWER, L.C. 2001-06-11 |