KAVO X PRO USB INTERFACE BOX

GUDID 06430035872961

PaloDEx Group Oy

Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental CAD/CAM system, chairside Dental milling system, CAD/CAM, chairside Dental milling system, CAD/CAM, chairside Dental milling system, CAD/CAM, chairside Dental milling system, CAD/CAM, chairside Dental milling system, CAD/CAM, chairside Dental milling system, CAD/CAM, chairside Dental milling system, CAD/CAM, chairside Dental milling system, CAD/CAM, chairside Dental milling system, CAD/CAM, chairside Dental milling system, CAD/CAM, chairside Dental milling system, CAD/CAM, chairside Dental milling system, CAD/CAM, chairside Dental milling system, CAD/CAM, chairside Dental milling system, CAD/CAM, chairside

• Primary Device ID: 06430035872961
• NIH Device Record Key: bf5a507e-0ce1-48c7-931a-65e6825688c4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KAVO X PRO USB INTERFACE BOX
• Version Model Number: 901123
• Company DUNS: 459955188
• Company Name: PaloDEx Group Oy
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06430035872961 [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: 2019-11-07
• Device Publish Date: 2019-10-30

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• 06430035875108 - ORTHOPANTOMOGRAPH™ OP 3D: 2023-10-10 ORTHOPANTOMOGRAPH™ OP 3D LX (PAN, CEPH 3D)
• 06430035873630 - Orthopantomograph OP 3D: 2021-06-08
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• 06430035874354 - Bite blocks 10pcs OP 3D: 2021-06-03
• 06430035874422 - CRANEX 3D PAT POSIT ACCESSORIES: 2021-06-03
• 06430035874439 - CRANEX 3D PAN ACCESSORIES: 2021-06-03