EkoSonic® 500-55140

GUDID 00858593006172

The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic Core. The device delivers physician-specified fluids and ultrasound to the intravascular treatment site. It comes in different working lengths and treatment zones.

EKOS CORPORATION

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Primary Device ID00858593006172
NIH Device Record Keyf9b31d1b-ebf8-4d2b-a08a-7924311792c0
Commercial Distribution StatusIn Commercial Distribution
Brand NameEkoSonic®
Version Model Number6779-006
Catalog Number500-55140
Company DUNS943488429
Company NameEKOS CORPORATION
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 Batchfalse
Serial Numbertrue
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

Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com
Phone888-400-3567
EmailEKOSCustomerService@ekoscorp.com

Device Dimensions

Length106 Centimeter
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter
Device Size Text, specify0
Length106 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100858593006172 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KRACatheter, Continuous Flush

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-10-23
Device Publish Date2016-09-23

On-Brand Devices [EkoSonic®]

00858593006509The Connector Interface Cable (CIC) is the cable assembly that connects the Infusion Catheter an
00858593006493The EkoSonic® Control Unit provides power to the Ultrasonic Core and monitors parameters during
00858593006318The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic
00858593006301The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic
00858593006295The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic
00858593006264The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic
00858593006189The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic
00858593006172The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic
00858593006165The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic
00858593006158The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic
00858593006141The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic
00858593006134The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic
00858593006028The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic

Trademark Results [EkoSonic]

Mark Image

Registration | Serial
Company
Trademark
Application Date
EKOSONIC
EKOSONIC
77569254 3608703 Live/Registered
EKOS Corporation
2008-09-12

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