Epix ® Inline Laparoscopic Dissector

GUDID 10607915124479

Disposable Dissector

APPLIED MEDICAL RESOURCES CORPORATION

Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

• Primary Device ID: 10607915124479
• NIH Device Record Key: 8ed26652-f3d8-4e72-b374-13c4eb540ec1
• Commercial Distribution Discontinuation: 2016-09-24
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Epix ® Inline Laparoscopic Dissector
• Version Model Number: CY050
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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

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

Device Dimensions

• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Length: 38 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 38 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 38 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 38 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 38 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 38 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 38 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 38 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 38 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 38 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 38 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 38 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 38 Centimeter
• Outer Diameter: 5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00607915124472 [Primary]
GS1	10607915124479 [Package]; Contains: 00607915124472; Package: [10 Units]; Discontinued: 2016-09-24; Not 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: 4
• Public Version Date: 2020-02-10
• Device Publish Date: 2016-09-24

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