3.3 VHO 903304340-0

GUDID 54014501505170

NARVA Lichtquellen GmbH + Co KG.

Ultraviolet tanning device

• Primary Device ID: 54014501505170
• NIH Device Record Key: 98f24b5c-79de-4d74-bd85-0cf9359529dc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3.3 VHO
• Version Model Number: FR71T12 3.3 VHO 160W
• Catalog Number: 903304340-0
• Company DUNS: 330119702
• Company Name: NARVA Lichtquellen GmbH + Co KG.
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com
• Phone: +1 781 331 0949
• Email: info@jwnorthamerica.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Attention: Fragile.

Device Identifiers

Device Issuing Agency	Device ID
GS1	04014501005170 [Primary]
GS1	54014501505170 [Package]; Contains: 04014501005170; Package: Tertiary Packaging [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: 2024-11-14
• Device Publish Date: 2024-11-06

On-Brand Devices [3.3 VHO ]

• 84014501004063: FR71T12 3.3 VHO 160W
• 54014501505170: FR71T12 3.3 VHO 160W