E-ON

GUDID 00366975003706

E-ON UNIVERSAL LIGHT-CURED COMPOSITE A2 0.25 CAPSULE SAMPLE

BENCO DENTAL SUPPLY CO.

Dental material injection cannula, reusable

• Primary Device ID: 00366975003706
• NIH Device Record Key: f650317b-c0c4-4c6b-b70b-12f7a0c23212
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: E-ON
• Version Model Number: 4662-082
• Company DUNS: 015108087
• Company Name: BENCO DENTAL SUPPLY CO.
• 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

Operating and Storage Conditions

• Storage Environment Temperature: Between 39 Degrees Fahrenheit and 73 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00366975003706 [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: 6
• Public Version Date: 2019-08-21
• Device Publish Date: 2016-11-11

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