BLUEPHASE POWERCURE 691918BU

GUDID DVIV691918BU1

Blueph. PowerCure & System Kit mixed

IVOCLAR VIVADENT AKTIENGESELLSCHAFT

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• Primary Device ID: DVIV691918BU1
• NIH Device Record Key: f2e6a176-6ab8-401c-b6c7-16afb5bb1c01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BLUEPHASE POWERCURE
• Version Model Number: 691918BU
• Catalog Number: 691918BU
• 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: false
• 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	DVIV691918BU1 [Primary]

FDA Product Code

• EBZ: ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION

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: 2021-12-10
• Device Publish Date: 2021-12-02

On-Brand Devices [BLUEPHASE POWERCURE]

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• DIVO7409981: Bluephase G4 handpiece, Bluephase G4 battery, Bluephase G4 light guide
• DVIV691918BU1: Blueph. PowerCure & System Kit mixed
• DVIV668253BU1: Bluephase PowerCure & System Kit syringe
• 07615208461299: Bluephase PowerCure 100-240V
• 07615208461251: Bluephase PowerCure 100-240V