Primary Device ID | G5100709 |
NIH Device Record Key | 0b21b87c-2fc8-42de-b945-eb7f34483a55 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MIDDAY SUN |
Version Model Number | 0709 |
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 | G5100709 [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 | 2024-10-07 |
Device Publish Date | 2024-09-27 |
G5101390 - SIGNATURE SERIES | 2024-10-14 |
G51020420 - HEX TRU TAN | 2024-10-14 |
G5103239 - HEX SMART | 2024-10-14 |
G5102872 - RAVE RUSH | 2024-10-11 |
G5100709 - MIDDAY SUN | 2024-10-07 |
G5100709 - MIDDAY SUN | 2024-10-07 |
G5100734 - NEVADA SUN | 2024-10-07 |
G5102956 - BRILLIANCE ADVANCED ACTIVE BRONZER | 2024-10-07 |
G5103230 - PURE SUNLIGHT | 2024-10-02 |