Echo

GUDID 00815871021258

Avante

Single-patient intensive/general healthcare physiologic monitoring system Single-patient intensive/general healthcare physiologic monitoring system Single-patient intensive/general healthcare physiologic monitoring system General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor

Primary Device ID	00815871021258
NIH Device Record Key	8d1409af-f3b5-4d0a-918b-7ceb9cec8625
Commercial Distribution Status	In Commercial Distribution
Brand Name	Echo
Version Model Number	60129B
Company DUNS	178440426
Company Name	Avante
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	false
Lot Batch	false
Serial Number	true
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Customer Support Contacts

Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com
Phone	502-244-4444
Email	devicehelp@dremed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00815871021258 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K102835

FDA Product Code

DQA

Oximeter

Sterilization

Steralize Prior To Use	false
Device Is Sterile	false

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	4
Public Version Date	2020-02-06
Device Publish Date	2016-09-23

On-Brand Devices [Echo]

00815871021968	60129NST
00815871021333	60129R
00815871021326	60129NS
00815871021319	60129NP
00815871021302	60129NC
00815871021296	60129CO2SDRS
00815871021289	60129CO2S
00815871021272	60129CO2
00815871021265	60129CN
00815871021258	60129B
00815871021241	60129AD
00815871021234	60129A
00815871021227	60129

Trademark Results [Echo]

Mark Image Registration \| Serial	Company Trademark Application Date
ECHO 98403638 not registered Live/Pending	Stylecraft, LLC 2024-02-13
ECHO 98298155 not registered Live/Pending	Ncardia B.V. 2023-12-04
ECHO 98242300 not registered Live/Pending	Foamtec International Co., Ltd. 2023-10-26
ECHO 98133210 not registered Live/Pending	Autism Solutions, Inc. 2023-08-15
ECHO 98092120 not registered Live/Pending	Tulster, LLC 2023-07-19
ECHO 98020509 not registered Live/Pending	Eastward Partners 2023-05-31
ECHO 97868610 not registered Live/Pending	Yen, Weixi 2023-04-01
ECHO 97759865 not registered Live/Pending	Amazon Technologies, Inc. 2023-01-18
ECHO 97756786 not registered Live/Pending	Echo Franchise Group, LLC 2023-01-17
ECHO 97756228 not registered Live/Pending	Echo Franchise Group, LLC 2023-01-16
ECHO 97740829 not registered Live/Pending	Rodney, Ryan 2023-01-04
ECHO 97720984 not registered Live/Pending	USA Beverage, LLC 2022-12-16