CORFLO Y Extension Set 40-1007

GUDID 20815149021731

Enteral feeding extension set.

CORPAK MEDSYSTEMS, INC.

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• Primary Device ID: 20815149021731
• NIH Device Record Key: ff899ff1-14de-4372-93e1-2a951d4ee970
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CORFLO Y Extension Set
• Version Model Number: 40-1007
• Catalog Number: 40-1007
• Company DUNS: 147530323
• Company Name: CORPAK MEDSYSTEMS, INC.
• Device Count: 1
• DM Exempt: true
• 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(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No

Device Identifiers

Device Issuing Agency	Device ID
GS1	10815149021734 [Primary]
GS1	20815149021731 [Package]; Contains: 10815149021734; Package: [30 Units]; In Commercial Distribution

FDA Product Code

• KNT: TUBES, GASTROINTESTINAL (AND ACCESSORIES)

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: 2023-07-31
• Device Publish Date: 2016-07-28

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