RapidPort EZ C-20390

GUDID 10811955020053

RapidPort EZ Applier Tool

Apollo Endosurgery, Inc.

Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator Infusion/injection port/tack applicator

• Primary Device ID: 10811955020053
• NIH Device Record Key: 89386506-d063-4ceb-9be3-b9a00f4dce4d
• Commercial Distribution Discontinuation: 2021-12-17
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: RapidPort EZ
• Version Model Number: C-20390
• Catalog Number: C-20390
• 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: 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: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10811955020053 [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: 5
• Public Version Date: 2021-12-30
• Device Publish Date: 2016-08-17

On-Brand Devices [RapidPort EZ]

• 10811955020299: RapidPort EZ Access Port Kit
• 10811955020282: RapidPort EZ Access Port Kit
• 10811955020053: RapidPort EZ Applier Tool