Cervitec F 745815AL

GUDID 07615208291551

Cervitec F Test Pack 3x0.26g

IVOCLAR VIVADENT AKTIENGESELLSCHAFT

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• Primary Device ID: 07615208291551
• NIH Device Record Key: 6505b99c-0fab-49bb-8df9-84f3b53d1e05
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cervitec F
• Version Model Number: 745815AL
• Catalog Number: 745815AL
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	07615208291551 [Primary]
HIBCC	DVIV745815AL1 [Previous]

FDA Product Code

• LBH: VARNISH, CAVITY

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: 2024-02-01
• Device Publish Date: 2024-01-24

On-Brand Devices [Cervitec F]

• DVIV665504AL0: Cervitec F Refill 20x0.26g
• DVIV745815AL1: Cervitec F Test Pack 3 x 0.26 g
• 07615208291551: Cervitec F Test Pack 3x0.26g