Golden Goddess Ultima 28012

GUDID 84014501004131

NARVA Lichtquellen GmbH + Co KG.

Ultraviolet tanning device

• Primary Device ID: 84014501004131
• NIH Device Record Key: ea550825-cedc-4a5d-8c86-134d28f46d98
• Commercial Distribution Discontinuation: 2025-09-18
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Golden Goddess Ultima
• Version Model Number: FR75 T12 100-120W
• Catalog Number: 28012
• 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

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.

Device Identifiers

Device Issuing Agency	Device ID
GS1	04014501004135 [Primary]
GS1	54014501404138 [Package]; Contains: 04014501004135; Package: Tertiary Packaging [24 Units]; Discontinued: 2025-09-18; Not in Commercial Distribution
GS1	84014501004131 [Package]; Contains: 54014501404138; Package: Pallet [24 Units]; Discontinued: 2025-09-18; Not 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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-09-19
• Device Publish Date: 2019-07-18

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