Primary Device ID | G51020500 |
NIH Device Record Key | 3f608e8e-ff41-466a-ad20-6997d058d488 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BERMUDA GOLD |
Version Model Number | 2050 |
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 | G51020500 [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 | 2024-06-21 |
Device Publish Date | 2024-06-13 |
G51014530 | 1453 |
G51019820 | 1982 |
G51020500 | 2050 |
G5101982 | 1982 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BERMUDA GOLD 85655107 not registered Dead/Abandoned |
JK North America, Inc. 2012-06-19 |
![]() BERMUDA GOLD 85654588 not registered Dead/Abandoned |
JK North America, Inc. 2012-06-18 |
![]() BERMUDA GOLD 79072491 3889279 Live/Registered |
JK-Holding GmbH 2009-02-20 |
![]() BERMUDA GOLD 78548389 3021018 Dead/Cancelled |
JK North America, Inc. 2005-01-16 |
![]() BERMUDA GOLD 78498905 3020782 Dead/Cancelled |
JK North America, Inc. 2004-10-13 |
![]() BERMUDA GOLD 78031300 not registered Dead/Abandoned |
Global Sun Light, Inc. 2000-10-18 |
![]() BERMUDA GOLD 72448964 0994076 Dead/Expired |
SOMERS DISTILLERS LTD. 1973-02-14 |