Brilliance Active Bronzer

GUDID G510196801

Light Sources, Inc.

Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device
Primary Device IDG510196801
NIH Device Record Keydd969f30-7618-40cc-a1f2-1593c3470001
Commercial Distribution StatusIn Commercial Distribution
Brand NameBrilliance Active Bronzer
Version Model Number1968
Company DUNS075058495
Company NameLight Sources, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCG510196801 [Primary]

FDA Product Code

LEJBooth, Sun Tan

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-05-16
Device Publish Date2024-05-08

On-Brand Devices [Brilliance Active Bronzer]

G5101968011968
G510282502825
G510241102411
G510292102921

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.