LAP-BAND B-20301

GUDID 20811955020418

LAP-BAND Access Port Needle 3.5 inch Pouch

Apollo Endosurgery, Inc.

Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle
Primary Device ID20811955020418
NIH Device Record Key3ba8d8fd-5ee6-4ad6-bb4a-9a03dd06a88e
Commercial Distribution StatusIn Commercial Distribution
Brand NameLAP-BAND
Version Model NumberB-20301
Catalog NumberB-20301
Company DUNS625064352
Company NameApollo Endosurgery, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com
Phone855-551-3123
Emailproductcomplaints.us@apollendo.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110811955020411 [Primary]
GS120811955020418 [Package]
Contains: 10811955020411
Package: Kit [10 Units]
In Commercial Distribution

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 Number5
Public Version Date2021-01-08
Device Publish Date2016-08-17

On-Brand Devices [LAP-BAND]

20811955020425LAP-BAND Access Port Needle 2 inch Pouch
20811955020418LAP-BAND Access Port Needle 3.5 inch Pouch
10811955020503LAP-BAND System Tubing Kit
10811955020374LAP-BAND System Calibration Tube
10811955020312The LAP-BAND AP Adjustable Gastric Banding System with RapidPort EZ
10811955020305The LAP-BAND AP Adjustable Gastric Banding System with RapidPort EZ

Trademark Results [LAP-BAND]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LAP-BAND
LAP-BAND
74600935 1937093 Live/Registered
APOLLO ENDOSURGERY US, INC.
1994-11-21

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