Universal Dentin Sealant 1020

GUDID 00883205104014

Universal Dentin Sealant Mini Kit Universal

ULTRADENT PRODUCTS, INC.

Dental coating, tooth-desensitizing

• Primary Device ID: 00883205104014
• NIH Device Record Key: d1568512-8fc2-4bc6-ab39-4e77509c3488
• Commercial Distribution Discontinuation: 2018-09-05
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Universal Dentin Sealant
• Version Model Number: 1020
• Catalog Number: 1020
• Company DUNS: 013369913
• Company Name: ULTRADENT PRODUCTS, INC.
• 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: true
• 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

Customer Support Contacts

• Phone: +1(801)572-4200
• Email: customerservice@ultradent.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 18 Degrees Celsius and 29 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00883205104014 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K963979

FDA Product Code

• LBH: VARNISH, CAVITY

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-02-07
• Device Publish Date: 2016-09-22

On-Brand Devices [Universal Dentin Sealant]

• 00883205104014: Universal Dentin Sealant Mini Kit Universal
• 00883205103338: Universal Dentin Sealant Kit
• 00883205103321: Universal Dentin Sealant Refill Universal