Valiant NA6050141

GUDID D707NA60501410

IVOCLAR VIVADENT, INC.

Dental amalgam

• Primary Device ID: D707NA60501410
• NIH Device Record Key: 5cb1f81f-3f0f-4290-9dde-571a1da17007
• Commercial Distribution Discontinuation: 2023-12-20
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Valiant
• Version Model Number: NA6050141
• Catalog Number: NA6050141
• Company DUNS: 176935203
• Company Name: IVOCLAR VIVADENT, INC.
• Device Count: 500
• 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: false
• 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	D707NA60501410 [Primary]
HIBCC	D707NA60501411 [Unit of Use]

FDA Product Code

• EJJ: Alloy, amalgam

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2023-12-21
• Device Publish Date: 2017-01-27

On-Brand Devices [Valiant]

• D707NA60501200: NA6050120
• D707NA60501400: NA6050140
• D707NA60501310: NA6050131
• D707NA60502410: Valiant Sure Cap No. 3 Econo
• D707NA60504211: Valiant Ph.D. No. 2 Econo
• D707NA60501410: NA6050141