Fred 2 220-50

GUDID 10884521066540

Anti-Fog Kit

Covidien LP

Endoscopic antifog solution Endoscopic antifog solution

• Primary Device ID: 10884521066540
• NIH Device Record Key: 70239f4c-cc64-4e38-888f-ced088d464d7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fred 2
• Version Model Number: 220-50
• Catalog Number: 220-50
• Company DUNS: 058614483
• Company Name: Covidien LP
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521066540 [Package]; Contains: 20884521066547; Package: CASE [20 Units]; In Commercial Distribution
GS1	20884521066547 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K923843

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: 2018-07-06
• Device Publish Date: 2016-09-24

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• 10884521539921 - VenaSeal: 2024-04-09 VenaSeal Closure System