BRIGHT FLOW CORE

GUDID 05206569851014

Dual curing flowable core build up composite

DMP DENTAL INDUSTRY S.A.

Dental composite resin

• Primary Device ID: 05206569851014
• NIH Device Record Key: 3fbfbcfa-620e-493a-bbfe-20835272742e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BRIGHT FLOW CORE
• Version Model Number: Universal, 25ml
• Company DUNS: 728534814
• Company Name: DMP DENTAL INDUSTRY S.A.
• 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: 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: +302299023041
• Email: info@dmpdental.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 4 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	05206569851014 [Primary]

FDA Product Code

• EBF: Material, Tooth Shade, Resin

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: 2016-09-24

On-Brand Devices [BRIGHT FLOW CORE]

• 05206569852011: Dual curing flowable core build up composite
• 05206569851014: Dual curing flowable core build up composite