Kerlix 2671

GUDID 20884521081649

Washed Gauze Bolt,3 Ply

Cardinal Health, Inc.

Woven gauze roll, non-sterile

• Primary Device ID: 20884521081649
• NIH Device Record Key: dec69767-07d6-49f4-8af0-d79e38d4ca9a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kerlix
• Version Model Number: 2671
• Catalog Number: 2671
• Company DUNS: 080935429
• Company Name: Cardinal Health, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

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

Device Dimensions

• Width: 9 Inch
• Length: 300 Feet
• Width: 9 Inch
• Length: 300 Feet

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *
• Special Storage Condition, Specify: Between 0 and 0 *

Device Identifiers

Device Issuing Agency	Device ID
GS1	20884521081649 [Primary]

FDA Product Code

• FRL: FIBER, MEDICAL, ABSORBENT

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-02-15
• Device Publish Date: 2018-06-23

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