VED-020

GUDID 50812496010198

Gravity Feed Transition Set with 40mm Screw Cap and ENFit Connector

METRIX COMPANY, THE

Enteral feeding kit, adult/paediatric, non-sterile Enteral feeding kit, adult/paediatric, non-sterile Enteral feeding bag/bottle Enteral feeding bag/bottle Enteral feeding bag/bottle Enteral feeding bag/bottle Enteral feeding bag/bottle Enteral feeding bag/bottle Enteral feeding bag/bottle Enteral feeding bag/bottle Enteral feeding bag/bottle

• Primary Device ID: 50812496010198
• NIH Device Record Key: ddc35a03-e6dd-4824-a100-45dba5d633c1
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: VED-020
• Catalog Number: VED-020
• Company DUNS: 043046283
• Company Name: METRIX COMPANY, THE
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812496010193 [Primary]
GS1	50812496010198 [Package]; Contains: 00812496010193; Package: Cardboard Carton [24 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132424

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: 2018-07-06
• Device Publish Date: 2016-11-30

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• 50812496011515 - SECURE®: 2019-10-23 EMPTY EVA DUAL CHAMBER CONTAINER WITH 5 PORT MANIFOLD FILL SET (8 SETS OF 5 BAGS)
• 50812496011539 - SECURE®: 2019-10-23 EMPTY EVA DUAL CHAMBER CONTAINER WITH 5 PORT MANIFOLD FILL SET (8 SETS OF 5 BAGS)