| Primary Device ID | 35019517091681 |
| NIH Device Record Key | d96f5b00-50d5-4392-bf32-c020d4cc7118 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ECHOGLO |
| Version Model Number | 24-4128-01 |
| Company DUNS | 082005361 |
| Company Name | Smiths Medical ASD, Inc. |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 15019517091687 [Primary] |
| GS1 | 35019517091681 [Package] Contains: 15019517091687 Package: Case [10 Units] In Commercial Distribution |
| BSP | NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-09-23 |
| Device Publish Date | 2020-09-15 |
| 35019517091681 | 24-4128-01 |
| 35019517091674 | 24-4127-01 |
| 35019517091667 | 24-4126-01 |
| 35019517091650 | 24-4122-01 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ECHOGLO 87686953 not registered Live/Pending |
Smiths Medical ASD, Inc. 2017-11-16 |
![]() ECHOGLO 85752562 4373747 Live/Registered |
Smiths Medical ASD, Inc. 2012-10-12 |