KaVo NOMAD Pro 2

GUDID D090101329300

KaVo NOMAD Pro 2, GBL

Dental Imaging Technologies Corporation

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• Primary Device ID: D090101329300
• NIH Device Record Key: ed27f1d9-0e77-4f17-a949-cf8c93e65048
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KaVo NOMAD Pro 2
• Version Model Number: 1.013.2930
• Company DUNS: 800111106
• Company Name: Dental Imaging Technologies Corporation
• 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: 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
HIBCC	D090101329300 [Primary]
HIBCC	EKAV101329300 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173319

FDA Product Code

• EHD: Unit, X-Ray, Extraoral With Timer

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: 2022-03-14
• Device Publish Date: 2022-03-04

On-Brand Devices [KaVo NOMAD Pro 2]

• D090101377880: KaVo NOMAD Pro 2, CA
• D090101329300: KaVo NOMAD Pro 2, GBL
• D090101329290: KaVo NOMAD Pro 2, US