| Primary Device ID | G51033220 |
| NIH Device Record Key | bd552a95-b7a8-43f8-a2d7-675647bb740c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ETERNAL SUN |
| Version Model Number | 3322 |
| 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 | G51033220 [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 | 2025-07-10 |
| Device Publish Date | 2025-07-02 |
| G51033220 | 3322 |
| G51033200 | 3320 |
| G51033240 | 3324 |
| G51033230 | 3323 |
| G51033210 | 3321 |
| G51033190 | 3319 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ETERNAL SUN 75810937 2548008 Live/Registered |
PC Marketing, Inc. 1999-09-29 |
![]() ETERNAL SUN 74422804 not registered Dead/Abandoned |
Schering-Plough HealthCare Products, Inc. 1993-08-10 |