Contour

GUDID 10841396117661

Self-Activating Capsule - Regular Set - Dispersed Phase Dental Amalgam - Triple Spill

KERR CORPORATION

Dental amalgam alloy

• Primary Device ID: 10841396117661
• NIH Device Record Key: a5cf1dc9-3fa1-48b0-9212-eb8386403568
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Contour
• Version Model Number: 29969
• Company DUNS: 847905890
• Company Name: KERR CORPORATION
• Device Count: 50
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com
• Phone: +18005377123
• Email: customercare@kavokerrgroup.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, well ventilated place

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841396117664 [Unit of Use]
GS1	10841396117661 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K820181

FDA Product Code

• EJJ: Alloy, amalgam

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-03-16
• Device Publish Date: 2016-08-31

On-Brand Devices [Contour]

• 10841396117739: Self-Activating Capsule - Fast Set - Dispersed Phase Dental Amalgam - Triple Spill
• 10841396117722: Self-Activating Capsule - Fast Set - Dispersed Phase Dental Amalgam - Triple Spill
• 10841396117715: Self-Activating Capsule - Fast Set - Dispersed Phase Dental Amalgam - Double Spill
• 10841396117708: Self-Activating Capsule - Fast Set - Dispersed Phase Dental Amalgam - Double Spill
• 10841396117692: Self-Activating Capsule - Fast Set - Dispersed Phase Dental Amalgam - Single Spill
• 10841396117685: Self-Activating Capsule - Fast Set - Dispersed Phase Dental Amalgam - Single Spill
• 10841396117678: Self-Activating Capsule - Regular Set - Dispersed Phase Dental Amalgam - Triple Spill
• 10841396117661: Self-Activating Capsule - Regular Set - Dispersed Phase Dental Amalgam - Triple Spill
• 10841396117654: Self-Activating Capsule - Regular Set - Dispersed Dental Amalgam - Double Spill
• 10841396117647: Self-Activating Capsule - Regular Set - Dispersed Phase Dental Amalgam - Double Spill
• 10841396117630: Self-Activating Capsule - Regular Set - Dispersed Dental Amalgam - Single Spill
• 10841396117623: Self-Activating Capsule - Regular Set - Dispersed Phase Dental Amalgam - Single Spill