CLEO 103913

GUDID B5331039131

BLV Licht- und Vakuumtechnik GmbH

Ultraviolet tanning device

• Primary Device ID: B5331039131
• NIH Device Record Key: 55c8c211-642e-4468-9629-f746cbadd703
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CLEO
• Version Model Number: HPA 400/30 SD L
• Catalog Number: 103913
• Company DUNS: 315736603
• Company Name: BLV Licht- und Vakuumtechnik 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: 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	B5331039130 [Primary]
HIBCC	B5331039131 [Package]; Contains: B5331039130; 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: 2020-03-10
• Device Publish Date: 2020-03-02

On-Brand Devices [CLEO ]

• B5331039441: HPA 1010 SE FX
• B5331039371: HPA 620 FX
• B5331039341: HPA 700 S FX
• B5331039131: HPA 400/30 SD L
• B5331039011: HPA 400/30 S L
• B5331038601: HPA 250-500 SE FX
• B5331038531: HPA 1200FX
• B5331141171: HPA 250-500 SE FX
• B5331141021: HPA 1010 SE FX
• B5331140520: HPA 1200FX
• B5331155040: HPA 620FX
• B5331181141: HPA 700 S FX
• B5331181061: HPA 400 S
• B5331181001: HPA 400/30 S L
• B5331180561: HPA 400/30 SD L
• B5331141521: HPA 610 FX
• B5331191500: Ultraviolet tanning device