ZINROC POWDER

GUDID 00850015110238

POWDER FOR MIXING WITH DENTAL CEMENT LIQUID

TEMREX CORPORATION

Zinc oxide eugenol dental cement

• Primary Device ID: 00850015110238
• NIH Device Record Key: 7353a2a2-9758-4316-aa37-866b9cf79798
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ZINROC POWDER
• Version Model Number: 440 White 100gm.
• 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	00850015110238 [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 [ZINROC POWDER]

• 00850015110269: POWDER FOR MIXING WITH DENTAL CEMENT LIQUID
• 00850015110252: POWDER FOR MIXING WITH DENTAL CEMENT LIQUID
• 00850015110245: POWDER FOR MIXING WITH DENTAL CEMENT LIQUID
• 00850015110238: POWDER FOR MIXING WITH DENTAL CEMENT LIQUID
• 00850015110221: POWDER FOR MIXING WITH DENTAL CEMENT LIQUID
• 00850015110214: POWDER FOR MIXING WITH DENTAL CEMENT LIQUID