Cervitec F 665504AL

GUDID DVIV665504AL0

Cervitec F Refill 20x0.26g

IVOCLAR VIVADENT AKTIENGESELLSCHAFT

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• Primary Device ID: DVIV665504AL0
• NIH Device Record Key: 6e4c22fc-4e21-48aa-bfc8-14c3d270ca69
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cervitec F
• Version Model Number: 665504AL
• Catalog Number: 665504AL
• Company DUNS: 448015938
• Company Name: IVOCLAR VIVADENT AKTIENGESELLSCHAFT
• Device Count: 20
• 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: 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
HIBCC	DVIV665504AL0 [Unit of Use]
HIBCC	DVIV665504AL1 [Primary]

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: 2021-03-30
• Device Publish Date: 2021-03-22

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