EON

GUDID 00366975002594

E-ON TOTAL cement , dental

BENCO DENTAL SUPPLY CO.

Dental composite resin

• Primary Device ID: 00366975002594
• NIH Device Record Key: 794f3712-3a8e-4c1e-ba0b-ba0199ba9bdd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EON
• Version Model Number: 4601-905
• Company DUNS: 015108087
• Company Name: BENCO DENTAL SUPPLY CO.
• 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

Operating and Storage Conditions

• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00366975002594 [Primary]

FDA Product Code

• EMA: Cement, Dental

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: 2016-09-23

On-Brand Devices [EON]

• 00366975013330: Eon Desensitizer without Glutaraldehyde
• 00366975013323: Eon Desensitizer with Glutaraldehyde
• 00366975002594: E-ON TOTAL cement , dental
• 00366975002587: E-ON SELF ETCH LC BOND AGENT
• 00366975036230: 5522-025