Enteral 1200 mL Gravity Feeding Bag

GUDID 38148440000839

ZEVEX INTERNATIONAL, INC.

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• Primary Device ID: 38148440000839
• NIH Device Record Key: ad945fe5-f790-4d1b-a982-78da7280507e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Enteral 1200 mL Gravity Feeding Bag
• Version Model Number: GR1200
• Company DUNS: 612746933
• Company Name: ZEVEX INTERNATIONAL, INC.
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com
• Phone: 800-970-2337
• Email: medcustomerservice@moog.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	18148440000835 [Primary]
GS1	38148440000839 [Package]; Contains: 18148440000835; 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: 2019-10-23
• Device Publish Date: 2016-10-21

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