Aquarius XH 579800

GUDID D7075798000

Aquarius XH 50 g

IVOCLAR VIVADENT, INC.

Dental casting noble alloy

• Primary Device ID: D7075798000
• NIH Device Record Key: eed63863-dc42-42ca-8baf-6d7c4cee7871
• Commercial Distribution Discontinuation: 2021-06-22
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Aquarius XH
• Version Model Number: 579800
• Catalog Number: 579800
• Company DUNS: 176935203
• Company Name: IVOCLAR VIVADENT, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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	D7075798000 [Primary]

FDA Product Code

• EJT: Alloy, gold-based noble metal

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-06-23
• Device Publish Date: 2018-10-29

On-Brand Devices [Aquarius XH]

• D7075798000: Aquarius XH 50 g
• D7075766160: Aquarius XH 100 g
• D7075766150: Aquarius XH 25 g
• D7075797990: Aquarius XH 1oz/31 g
• D7075797970: Aquarius XH 5 g