TEMREX LIQUID

GUDID 00850015110023

LIQUID FOR MIXING WITH DENTAL CEMENT POWDER

TEMREX CORPORATION

Zinc oxide eugenol dental cement

• Primary Device ID: 00850015110023
• NIH Device Record Key: 989da724-d07b-4433-bc05-a45728042590
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TEMREX LIQUID
• Version Model Number: 310 1oz.
• Company DUNS: 012072823
• Company Name: TEMREX CORPORATION
• 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: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850015110023 [Primary]

FDA Product Code

• EMA: Cement, Dental

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: 2020-02-21
• Device Publish Date: 2020-02-13

On-Brand Devices [TEMREX LIQUID]

• 00850015110108: Powder for Mixing with Dental Cement Liquid
• 00850015110023: LIQUID FOR MIXING WITH DENTAL CEMENT POWDER