ProVecta 3D Prime Ceph

GUDID E2472210200729

DÜRR DENTAL SE

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• Primary Device ID: E2472210200729
• NIH Device Record Key: 84863c04-edb5-4a15-8bd0-5867165baca2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProVecta 3D Prime Ceph
• Version Model Number: 2210200729
• Company DUNS: 315563684
• Company Name: DÜRR DENTAL SE
• 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: 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
HIBCC	E2472210200729 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K193139

FDA Product Code

• OAS: X-Ray, Tomography, Computed, Dental

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: 2020-03-17
• Device Publish Date: 2020-03-09

On-Brand Devices [ProVecta 3D Prime Ceph]

• E2472210200729: 2210200729
• E247A78500: X-Ray System
• E247A78610: X-Ray System