Kalfasun 114210

GUDID B5331142101

BLV Licht- und Vakuumtechnik GmbH

Ultraviolet tanning device

• Primary Device ID: B5331142101
• NIH Device Record Key: a0b1ecb3-08ba-4093-abc9-264b917c4c53
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kalfasun
• Version Model Number: Kalfasun 630 FDA
• Catalog Number: 114210
• 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	B5331142100 [Primary]
HIBCC	B5331142101 [Package]; Contains: B5331142100; 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: 2023-06-21
• Device Publish Date: 2023-06-13

On-Brand Devices [Kalfasun]

• B5331165151: Kalfasun 1540 FDA
• B5331157300: Kalfasun 1510 FDA
• B5331152711: Kalfasun 640 FDA
• B5331142101: Kalfasun 630 FDA
• B5331142091: Kalfasun 610 FDA
• B5331140451: Kalfasun 1530 FDA