CLEO HPA 913103645

GUDID G6199131036451

Ultraviolet tanning device

JW NORTH AMERICA, INC.

Ultraviolet tanning device
Primary Device IDG6199131036451
NIH Device Record Keyb4b08431-6ae0-47cc-b8e6-13bb1ed9934e
Commercial Distribution StatusIn Commercial Distribution
Brand NameCLEO HPA
Version Model Number1200 FX
Catalog Number913103645
Company DUNS039280558
Company NameJW NORTH AMERICA, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB5331140520 [Previous]
HIBCCG6199131036450 [Primary]
HIBCCG6199131036451 [Package]
Contains: G6199131036450
Package: carton box [25 Units]
In Commercial Distribution

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 Date2024-08-09
Device Publish Date2024-08-01

On-Brand Devices [CLEO HPA]

G6199386702451Ultraviolet tanning device
G6199213785411Ultraviolet tanning device
G6199213761451Ultraviolet tanning device
G6199206749311Ultraviolet tanning device
G6199206695411Ultraviolet tanning device
G6199192202451Ultraviolet tanning device
G6199131388411Ultraviolet tanning device
G6199131371411Ultraviolet tanning device
G6199131340451Ultraviolet tanning device
G6199131036451Ultraviolet tanning device

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