ERGOLINE 114062

GUDID B5331140621

BLV Licht- und Vakuumtechnik GmbH

Ultraviolet tanning device

• Primary Device ID: B5331140621
• NIH Device Record Key: 6c0c427b-c122-4655-a7f8-a746859d76aa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ERGOLINE
• Version Model Number: JK 60/80 EF
• Catalog Number: 114062
• 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	B5331140620 [Primary]
HIBCC	B5331140621 [Package]; Contains: B5331140620; 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: 2020-12-15
• Device Publish Date: 2020-12-07

On-Brand Devices [ERGOLINE]

• B5331038591: ULTRA 520W
• B5331037511: JK 60/80 EF
• B5331141161: ULTRA 520W
• B5331140621: JK 60/80 EF