Primary Device ID | G51021350 |
NIH Device Record Key | e00b529e-e099-4008-aad8-c279a75a942b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SUN MASTER |
Version Model Number | 2135 |
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 | G51021350 [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 | 2024-05-17 |
Device Publish Date | 2024-05-09 |
G51021560 | SUNMASTER CLEARTECH 20 F71/HO/BP/ SOL65 GR |
G51024860 | 2486 |
G51024850 | 2485 |
G51021370 | 2137 |
G51021350 | 2135 |
G51019600 | 1960 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() SUN MASTER 85077223 3959827 Live/Registered |
Lumite, Inc. 2010-07-02 |
![]() SUN MASTER 76598586 not registered Dead/Abandoned |
THE AWNING WAREHOUSE, INC. 2004-06-21 |
![]() SUN MASTER 74258279 1772369 Live/Registered |
SUMMIT HILL, INC. 1992-03-23 |
![]() SUN MASTER 73625519 1469066 Dead/Cancelled |
HOME & ROAM LEISURE, INC. 1986-10-16 |
![]() SUN MASTER 73366775 1260933 Live/Registered |
California Umbrella Sales, Inc. 1982-05-27 |
![]() SUN MASTER 73254776 1164668 Dead/Cancelled |
Louverdrape, Inc. 1980-03-20 |