| Primary Device ID | 00858593006172 |
| NIH Device Record Key | f9b31d1b-ebf8-4d2b-a08a-7924311792c0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EkoSonic® |
| Version Model Number | 6779-006 |
| Catalog Number | 500-55140 |
| 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 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 | 00858593006172 [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 |