IPS e.max ZirCAD 725180

GUDID 07615208479058

IPS e.max ZirCAD Prime B2 98.5-14/1

IVOCLAR VIVADENT AKTIENGESELLSCHAFT

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• Primary Device ID: 07615208479058
• NIH Device Record Key: 69bedb93-3427-4eb6-a47c-59e9b8fadf00
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IPS e.max ZirCAD
• Version Model Number: 725180
• Catalog Number: 725180
• Company DUNS: 448015938
• Company Name: IVOCLAR VIVADENT AKTIENGESELLSCHAFT
• 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: 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	07615208479058 [Primary]

FDA Product Code

• EIH: POWDER, PORCELAIN

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: 2024-02-29
• Device Publish Date: 2024-02-21

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