| Primary Device ID | G51026650 |
| NIH Device Record Key | 176d52c2-bf0a-4389-a3d6-0344e92c0d45 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AUVL |
| Version Model Number | 2665 |
| 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 | G51026650 [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 | 2024-05-23 |
| Device Publish Date | 2024-05-15 |
| G51026650 | 2665 |
| G51016970 | 1697 |
| G5102483 | 2483 |
| G51032290 | 3229 |
| G51026640 | 2664 |
| G51019070 | F74T12/BL/HO/RDC/8.5B |
| G5103334 | 3334 |
| G5103336 | 3336 |
| G5103335 | 3335 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() AUVL 86867086 5324492 Live/Registered |
G.L.E. GESELLSCHAFT FÃR LICHTTECHNISCHEERZEUGNISSE MBH 2016-01-06 |
![]() AUVL 85502149 4356282 Live/Registered |
G.L.E. GESELLSCHAFT FÃR LICHTTECHNISCHEERZEUGNISSE MBH 2011-12-22 |
![]() AUVL 78369114 2930788 Live/Registered |
SUPERIOR UV TECHNOLOGIES, LLC 2004-02-17 |