Access Port RapidPort EZ Kit B-2306

GUDID 10811955020251

RAPIDPORT EZ Access Port Kit 14CC

Apollo Endosurgery, Inc.

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Primary Device ID10811955020251
NIH Device Record Key8c589757-4744-4e74-8a05-347e1ec483c1
Commercial Distribution Discontinuation2021-12-17
Commercial Distribution StatusNot in Commercial Distribution
Brand NameAccess Port RapidPort EZ Kit
Version Model NumberB-2306
Catalog NumberB-2306
Company DUNS625064352
Company NameApollo Endosurgery, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com
Phone855-551-3123
EmailProductSupport@allergan.com

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS110811955020251 [Primary]

FDA Product Code

LTIImplant, Intragastric For Morbid Obesity

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-12-30
Device Publish Date2014-08-26

Devices Manufactured by Apollo Endosurgery, Inc.

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00811955020933 - Apollo ESG NXT System2023-11-24 Single Channel Endobariatric System
00811955020940 - Apollo Revise NXT System2023-11-24 Single Channel Endobariatric System
00811955020780 - APOLLO ESG™ System2023-05-15 Dual Channel Endobariatric System
00811955020797 - APOLLO ESG Sx™ System2023-05-15 Single Channel Endobariatric System
00811955020803 - APOLLO Revise™ System2023-05-15 Dual Channel Endobariatric System
00811955020810 - APOLLO REVISE™ Sx System2023-05-15 Single Channel Endobariatric System

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