CLEO HPA 920674931

GUDID G6199206749311

Ultraviolet tanning device

Primary Device ID	G6199206749311
NIH Device Record Key	d312a8a0-2145-47b8-9f46-428b1b758758
Commercial Distribution Status	In Commercial Distribution
Brand Name	CLEO HPA
Version Model Number	700/800 FX C
Catalog Number	920674931
Company DUNS	039280558
Company Name	JW NORTH AMERICA, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
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	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	true

Device Issuing Agency	Device ID
HIBCC	B5331191500 [Previous]
HIBCC	G6199206749310 [Primary]
HIBCC	G6199206749311 [Package] Contains: G6199206749310 Package: carton box [25 Units] In Commercial Distribution

LEJ	Booth, Sun Tan

Steralize Prior To Use	false
Device Is Sterile	false