Primary Device ID | 00858593006165 |
NIH Device Record Key | 39ae8dc3-6b9b-40d4-820b-e2da27b969b4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EkoSonic® |
Version Model Number | 6779-005 |
Catalog Number | 500-55130 |
Company DUNS | 943488429 |
Company Name | EKOS CORPORATION |
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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Length | 106 Centimeter |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Size Text, specify | 0 |
Length | 106 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00858593006165 [Primary] |
KRA | Catheter, Continuous Flush |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2016-09-23 |
00858593006509 | The Connector Interface Cable (CIC) is the cable assembly that connects the Infusion Catheter an |
00858593006493 | The EkoSonic® Control Unit provides power to the Ultrasonic Core and monitors parameters during |
00858593006318 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic |
00858593006301 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic |
00858593006295 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic |
00858593006264 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic |
00858593006189 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic |
00858593006172 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic |
00858593006165 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic |
00858593006158 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic |
00858593006141 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic |
00858593006134 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic |
00858593006028 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EKOSONIC 77569254 3608703 Live/Registered |
EKOS Corporation 2008-09-12 |