Primary Device ID | G51031380 |
NIH Device Record Key | 083143af-f043-4f3d-88b7-b409f48b041f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SOLAR BRONZE |
Version Model Number | 3138 |
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 | G51031380 [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 | 2024-05-31 |
Device Publish Date | 2024-05-23 |
G51031480 | 3148 |
G51031460 | 3146 |
G51031380 | 3138 |
G51031360 | 3136 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() SOLAR BRONZE 87942949 not registered Live/Pending |
JLW-TW Corp 2018-05-31 |
![]() SOLAR BRONZE 75208191 2130259 Dead/Cancelled |
Vickmark Industries, L.L.C. 1996-11-20 |