Embonte +

GUDID 00814978024353

Zinc Oxide Eugenol Temporary Cement Dual Barrel Syringe

Kerr Corporation

Fatty acid dental cement

• Primary Device ID: 00814978024353
• NIH Device Record Key: 80b317be-4792-44ed-b454-48c356f89e5d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Embonte +
• Version Model Number: 27200DX
• Company DUNS: 199354556
• Company Name: Kerr 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: 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: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com

Device Dimensions

• Weight: 15 Gram
• Weight: 15 Gram

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at room temperature

Device Identifiers

Device Issuing Agency	Device ID
GS1	00814978024353 [Primary]

FDA Product Code

• EMB: ZINC OXIDE EUGENOL

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: 2017-08-31

On-Brand Devices [Embonte +]

• 00814978024353: Zinc Oxide Eugenol Temporary Cement Dual Barrel Syringe
• 00814978024346: Zinc Oxide Eugenol Temporary Cement Automix Syringe