RapidPort EZ Tubing Kit A-20331

GUDID 10811955020077

RAPIDPORT EZ Tubing Kit

Apollo Endosurgery, Inc.

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• Primary Device ID: 10811955020077
• NIH Device Record Key: 287906c0-1ad0-4ca8-a15c-0891e6ccbbbd
• Commercial Distribution Discontinuation: 2021-12-17
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: RapidPort EZ Tubing Kit
• Version Model Number: A-20331
• Catalog Number: A-20331
• Company DUNS: 625064352
• Company Name: Apollo Endosurgery, 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• 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: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apollendo.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10811955020077 [Primary]

FDA Product Code

• LTI: Implant, Intragastric For Morbid Obesity

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: 2021-12-30
• Device Publish Date: 2014-08-26

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