Voyant Maryland Fusion Device with Single-Step Activation

GUDID 00607915140809

Voyant Maryland Fusion Device with Single-Step Activation

APPLIED MEDICAL RESOURCES CORPORATION

Electrosurgical system

• Primary Device ID: 00607915140809
• NIH Device Record Key: d0b80589-719f-4ba9-8006-3384b9f750fc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Voyant Maryland Fusion Device with Single-Step Activation
• Version Model Number: EB213
• Company DUNS: 187129135
• Company Name: APPLIED MEDICAL RESOURCES CORPORATION
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com

Device Dimensions

• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 44 Centimeter
• Outer Diameter: 5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00607915140809 [Primary]
GS1	10607915140806 [Package]; Package: [6 Units]; In Commercial Distribution

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-04-04
• Device Publish Date: 2022-12-13

On-Brand Devices [Voyant Maryland Fusion Device with Single-Step Activation]

• 10607915140813: Electrosurgical Sealer and Divider handpiece
• 00607915140809: Voyant Maryland Fusion Device with Single-Step Activation
• 10607915140790: Electrosurgical Sealer and Divider handpiece