FONA ART Plus C 9768263121

GUDID E3158468463121

FONA SRL

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• Primary Device ID: E3158468463121
• NIH Device Record Key: c3dfd9c1-8809-440d-861a-483a000ef31a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FONA ART Plus C
• Version Model Number: 8468463121
• Catalog Number: 9768263121
• Company DUNS: 514320345
• Company Name: FONA SRL
• 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: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E3158468463121 [Primary]

FDA Product Code

• MUH: System, X-Ray, Extraoral Source, Digital

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: 2023-06-20
• Device Publish Date: 2023-06-12

On-Brand Devices [FONA ART Plus C]

• E3158468463221: 8468463221
• E3158468463121: 8468463121