Porcelain Repair 1108

GUDID 00883205103093

Porcelain Repair Kit

ULTRADENT PRODUCTS, INC.

Dental etching solution

• Primary Device ID: 00883205103093
• NIH Device Record Key: cdb8ee07-336e-4002-aba5-2a58d52d4270
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Porcelain Repair
• Version Model Number: 1108
• Catalog Number: 1108
• 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 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00883205103093 [Primary]

FDA Product Code

• EIH: POWDER, PORCELAIN

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: 2018-03-29
• Device Publish Date: 2016-09-22

On-Brand Devices [Porcelain Repair]

• 00883205103093: Porcelain Repair Kit
• 00883205034465: Porcelain Repair Kit