CORFLO Gastrostomy Tube 52-2024

GUDID 20815149021083

Dual Gastrostomy tube with ENFit Connectors

CORPAK MEDSYSTEMS, INC.

Gastrostomy tube

• Primary Device ID: 20815149021083
• NIH Device Record Key: c7352f0a-810d-402f-9a06-d8a0ec69013a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CORFLO Gastrostomy Tube
• Version Model Number: 52-2024
• Catalog Number: 52-2024
• 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

Device Dimensions

• Total Volume: 20 Milliliter

Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10815149021086 [Primary]
GS1	20815149021083 [Package]; Contains: 10815149021086; Package: [2 Units]; In Commercial Distribution

FDA Product Code

• KNT: TUBES, GASTROINTESTINAL (AND ACCESSORIES)

Sterilization

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

[20815149021083]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-04-20
• Device Publish Date: 2016-06-24

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