Voyant Maryland Fusion Device with Single-Step Activation

GUDID 10607915140813

Electrosurgical Sealer and Divider handpiece

APPLIED MEDICAL RESOURCES CORPORATION

Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system Electrosurgical system

• Primary Device ID: 10607915140813
• NIH Device Record Key: aa16257d-7276-48e9-9a36-3afcabeb6782
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Voyant Maryland Fusion Device with Single-Step Activation
• Version Model Number: EB214
• 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: 23 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 23 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 23 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 23 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 23 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 23 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 23 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 23 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 23 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 23 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 23 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 23 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 23 Centimeter
• Outer Diameter: 5 Millimeter
• Shaft Length: 23 Centimeter
• Outer Diameter: 5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00607915140816 [Primary]
GS1	10607915140813 [Package]; Contains: 00607915140816; 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