EON

GUDID 00366975036230

BENCO DENTAL SUPPLY CO.

Dental amalgam mixer

• Primary Device ID: 00366975036230
• NIH Device Record Key: fe26e675-71f7-415a-b55a-0dc1d777e055
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EON
• Version Model Number: 5522-025
• 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: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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	00366975036230 [Primary]

FDA Product Code

• EFD: Amalgamator, Dental, Ac-Powered

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: 2022-08-12
• Device Publish Date: 2022-08-04

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