ORIGINAL HANAU 80038171

GUDID G619800381711

Ultraviolet tanning device

JW NORTH AMERICA, INC.

Ultraviolet tanning device

• Primary Device ID: G619800381711
• NIH Device Record Key: 1dca8d83-51bf-489e-8d8f-60d785e184a8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ORIGINAL HANAU
• Version Model Number: OH N 800 ECF
• Catalog Number: 80038171
• 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 Identifiers

Device Issuing Agency	Device ID
HIBCC	G619800381710 [Primary]
HIBCC	G619800381711 [Package]; Contains: G619800381710; Package: carton box [25 Units]; In Commercial Distribution

FDA Product Code

• LEJ: Booth, Sun Tan

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-11
• Device Publish Date: 2024-11-01

On-Brand Devices [ORIGINAL HANAU]

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• G619800231081: Ultraviolet tanning device
• G619800215171: Ultraviolet tanning device
• G619800153561: Ultraviolet tanning device
• G619800153551: Ultraviolet tanning device
• G619800098981: Ultraviolet tanning device
• G619800085991: Ultraviolet tanning device
• G619800044571: Ultraviolet tanning device
• G619560698991: Ultraviolet tanning device
• G619450065491: Ultraviolet tanning device
• G619450065441: Ultraviolet tanning device
• G619450064111: Ultraviolet tanning device
• G619450064091: Ultraviolet tanning device