Safefeed

GUDID 10813153021672

Safefeed Enteral Reservoir

CODAN US CORPORATION

Enteral tube extension, sterile

• Primary Device ID: 10813153021672
• NIH Device Record Key: 6ba1168a-7903-4bc0-804a-f937a88e7636
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Safefeed
• Version Model Number: EF 130
• Company DUNS: 058027475
• Company Name: CODAN US 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813153021675 [Package]; Package: [1 Units]; In Commercial Distribution
GS1	10813153021672 [Primary]

FDA Product Code

• KNT: Tubes, Gastrointestinal (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: 2020-02-07
• Device Publish Date: 2016-09-20

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