KAVO LS3

GUDID 04260592020022

Optical 3D Scanner

smart optics Sensortechnik GmbH

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• Primary Device ID: 04260592020022
• NIH Device Record Key: 6a12af1e-4bd0-4763-8982-e3cc005d35be
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KAVO LS3
• Version Model Number: Demo Scanner 0.870.0200
• Company DUNS: 388004710
• Company Name: smart optics Sensortechnik GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260592020022 [Primary]

FDA Product Code

• NOF: System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations

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: 2018-04-13
• Device Publish Date: 2018-03-13

On-Brand Devices [KAVO LS3]

• 04260592020039: Optical 3D Scanner
• 04260592020022: Optical 3D Scanner
• 04260592020015: Optical 3D Scanner