Viper EVI1011

GUDID EAMIEVI10111

AMI Agency for Medical Innovations GmbH

Endoscopic electrosurgical electrode, monopolar, single-use

• Primary Device ID: EAMIEVI10111
• NIH Device Record Key: 8e76ee3a-c8a7-4836-98ee-af95828900b4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Viper
• Version Model Number: EVI1011
• Catalog Number: EVI1011
• Company DUNS: 303655286
• Company Name: AMI Agency for Medical Innovations GmbH
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 45 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EAMIEVI10110 [Primary]
HIBCC	EAMIEVI10111 [Package]; Contains: EAMIEVI10110; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K182013

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-04-15
• Device Publish Date: 2019-04-05

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