Epix Laparoscopic Scissors

GUDID 10607915110137

Laparoscopic Scissors

APPLIED MEDICAL RESOURCES CORPORATION

Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

• Primary Device ID: 10607915110137
• NIH Device Record Key: 646a1d51-37b2-4732-8b65-d1ed1eb44f7a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Epix Laparoscopic Scissors
• Version Model Number: CB040
• 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: false
• 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
• 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

• Lumen/Inner Diameter: 5 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter
• Length: 45 Centimeter
• Lumen/Inner Diameter: 5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00607915110130 [Primary]
GS1	10607915110137 [Package]; Contains: 00607915110130; Package: [10 Units]; In Commercial Distribution
GS1	10607915143012 [Package]; Contains: 00607915110130; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• HET: Laparoscope, Gynecologic (And 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: 3
• Public Version Date: 2019-02-21
• Device Publish Date: 2016-09-24

On-Brand Devices [Epix Laparoscopic Scissors]

• 10607915110137: Laparoscopic Scissors
• 10607915110120: Laparoscopic Scissors