KBL 6700 alpha

GUDID 04260489020081

This device is an over-the-counter tanning device emitting ultraviolet light in the UVB and UVA region of the spectrum intended for tanning of the hu

KBL GmbH

Ultraviolet tanning device

• Primary Device ID: 04260489020081
• NIH Device Record Key: bea0102a-873d-4bd7-a717-8dc51c3b48a6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KBL 6700 alpha
• Version Model Number: KBL 6808 - 46/4a 1616 cpi_us
• Company DUNS: 341936227
• Company Name: KBL GmbH
• 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: false
• Serial Number: true
• Manufacturing Date: true
• 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
GS1	04260489020081 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K151962

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: 4
• Public Version Date: 2018-08-06
• Device Publish Date: 2017-02-09

On-Brand Devices [KBL 6700 alpha]

• 04260489020098: This device is an over-the-counter tanning device emitting ultraviolet light in the UVB and UVA
• 04260489020081: This device is an over-the-counter tanning device emitting ultraviolet light in the UVB and UVA